Clinical Research Associate Resume Samples

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S Donnelly

Sven

Donnelly

64789 Meaghan Avenue

Phoenix

+1 (555) 512 2584

64789 Meaghan Avenue

Phoenix

Phone

p +1 (555) 512 2584

Experience Experience

New York, NY

Clinical Research Associate

New York, NY

Farrell-Schmeler

New York, NY

Clinical Research Associate

Make recommendations for improvements to your Manager
Participate in the performance appraisal program by providing timely and accurate feedback regarding the performance of a perspective CRA
Independently performs CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems
Reviews clinical data/information and oversees data correction. Assists study managers in providing interim and final reports and presentations
Works under supervision to manage work flow to accomplish assigned objectives
May provide assistance to the Clinical Project Manager and/or CRS with design of study tools, documents and processes
Working with management to develop project-specific CRA training

Dallas, TX

Lead Clinical Research Associate

Dallas, TX

Cassin, Bosco and Pouros

Dallas, TX

Lead Clinical Research Associate

Assists the Project Manager/Clinical Trial Manager with UAT testing and eCRF guideline review
Monitors site performance and compliance and provide management with necessary reports, updates and recommendations
Develops Clinical Monitoring Plans with review from the CRA Manager
Assists in evaluation of vendor performance during conduct of the study
Assists in the preparation and review of protocols, eCRFs, study manuals, and other study documents as requested by Clinical Trial Manager
Tracks utilization of visits against the budget in conjunction with the study Project Manager/Clinical Trial Manager
Develops Monitoring tools, Source Document Templates, and trip report annotations with review from the CRA Manager

present

Houston, TX

Senior Clinical Research Associate

Houston, TX

Hegmann, Padberg and Gerhold

present

Houston, TX

Senior Clinical Research Associate

present

Arranging on-site visits and logistics
Providing microbiology lab support to clinical programs
Supporting Product Development Lab with In House Clinical Study (ICS) screening and verification testing during development
Conducting study site feasibility assessments and qualification visits
Managing and coordinating cross-functional project teams
Serving as the primary project contact with the Sponsor (Customer)
Monitoring team performance against contract, customer expectations, and project baselines

Education Education

Bachelor’s Degree in Science

California State University, Northridge

Bachelor’s Degree in Science

Skills Skills

Excellent knowledge of Good Clinical Practice (GCP) and also good working knowledge of conducting clinical trials in general
Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software
Demonstrated ability to attain and maintain a working knowledge of Good Clinical Practices and applicable Standard Operating Procedures
Project management experience including the ability to prioritize, plan & evaluate deliverables; is well organized and structured, strong attention to detail
Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
Demonstrated ability to attain and maintain a working knowledge of GCPs and applicable SOPs
Comfortable with technology and ability to learn new systems quickly
Excellent understanding and demonstrated application of Good Clinical Practices and applicable Standard Operating Procedures
Attention to detail and the ability to prioritize. Strong organizational, planning and follow-through skills
Demonstrated ability to evaluate medical research data and proficient knowledge of medical terminology

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15 Clinical Research Associate resume templates

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Lead Clinical Research Associate Resume Examples & Samples

Prior Oncology experience
Strong experience with EDC systems experience
Able to demonstrate the critical elements of GCPs and federal regulations as it relates to clinical monitoring, IRB and Investigator responsibilities
CCRA certification

Senior Clinical Research Associate Resume Examples & Samples

At least 6 years of experience in clinical research
Bachelor's Degree or higher, scientific discipline is preferred
Thorough understanding of drug development

Senior Clinical Research Associate Resume Examples & Samples

4-6 years industry experience, including a minimum 4 years clinical research experience
Competent in the skills for the CRA II
Experience in line management and/or mentoring of CR Assistants and CRAs
Contributes in process improvement teams
Understanding of the clinical development plan and how the individual
Bachelor’s degree in biological science preferred
Combination of educational and work experience providing competencies to perform the required accountabilities specific to position

Senior Clinical Research Associate Resume Examples & Samples

3-5 years of CRA experience
IVD experience is preferred
Operational expertise
Experienced in presenting study-related material
Experienced in writing professional emails to both internal and external customers
Oncology clinical trial experience highly preferred
Laboratory/Med Tech background highly desirable
Bachelor's or Masters in Biology, Chemistry, Molecular Biology or related discipline
Global study experience/experience managing sites located in Europe/Asia
Ability to work in a team situation
Budget and contract development
Ability to solve problems in a detailed, comprehensive manner with demonstrated urgency and energy to handle problems
Must meet timelines and manage sites
MSWord, Excel and PowerPoint skills are required
Experience developing professional presentations and presenting to investigational sites and management

Clinical Research Associate Resume Examples & Samples

Bachelor’s degree in Biology or related discipline
1+ years of experience within the biotechnology or pharmaceutical industry; drug development experience preferred
Working knowledge of good clinical practices (GCP)
Proficiency in Microsoft Office Suite

Senior Clinical Research Associate Resume Examples & Samples

Bachelor’s degree in a science-related discipline and/or Registered Nurse licensure required
2+ years as a clinical research monitor; dermatology experience preferred
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Demonstrated understanding of Good Clinical Practices and Standard Operating Procedures
Flexibility to travel domestically up to 60-80% as required

Senior Clinical Research Associate Resume Examples & Samples

Bachelor’s degree in a scientific discipline and/or certification in a related allied health profession (e.g., nursing certification, medical or laboratory technology)
4+ years of clinical research monitoring experience; 3+ years of oncology experience preferred
Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements
Understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs

Clinical Research Associate Resume Examples & Samples

3+ years of experience as Clinical Research Associate; experience in early development trials preferred
Bachelor’s degree in Biology, Pharmacy, or similar health-related discipline
Strong regulatory knowledge (including GCP)
Flexibility to travel up to 65% domestically

Lead Clinical Research Associate Resume Examples & Samples

4+ years of relevant industry experience in a CRO, pharmaceutical company or biotechnology company
Comprehensive understanding of all aspects of clinical trial documentation, including Clinical Study Report compilation
Strong familiarity with industry standards as applied to ICH guidelines, GCP, and the CFR
Working knowledge of clinical monitoring responsibilities and procedures

Senior Clinical Research Associate Resume Examples & Samples

3+ years of Clinical Research (CRA) and/or Clinical Research Management experience with demonstrated experience in multi-national and/or multi-site clinical studies; 3+ years of experience working as a Clinical Trial Coordinator as part of a research team in a Hospital
Experience with ultrasound contrast agents
Working knowledge of GCPs, CFR, and ICH guidelines
Experience in diagnostic imaging field

Senior Clinical Research Associate Resume Examples & Samples

5+ years of experience in Pharmaceutical Clinical Research
Associate's Degree in a Scientific / Healthcare field
Extensive knowledge of ICH/GCP guidelines and regulatory requirements
Respiratory experience

Clinical Research Associate Resume Examples & Samples

Partners with CAPMs and project team members to perform initial contact with potential investigators and participates in the assessment and selection of qualified investigators for inclusion in research
Performs Qualification, Initiation, Monitoring,
Works with research site personnel to ensure all research activities are run compliantly and according to protocol
Perform comprehensive site management activities. Provide high-level consultative services to site personnel by coordinating and disseminating all pertinent data regarding study protocols, Case Report Forms, and GCP/applicable regulatory guidelines. Help to define quality standards within the project team
Reviews study documentation such as protocols, informed consents, amendments, case report forms and study reports
Reviews ethics committee reports
Ensures compliant recording and reporting of
Bachelor’s degree (or internationally recognized equivalent) in a life sciences related field or R.N. with a minimum of 2 years experience with clinical research, OR minimum of 6 years progressive experience with clinical research
Clinical Research experience such as: study site research coordination or management; sponsor-level clinical research project team experience. Other experience may include investigator qualifications; study monitoring; Clinical QA Auditing and/or Clinical Data Management within the pharmaceutical or medical device industry. (Medical Device research preferred.)
Good collaborative oral and written communication skills, with ability to relay pertinent information to site personnel and study teams
Strong team skills with ability to work effectively with GEHC and research site personnel
Ability to travel up to 70% of time for job related responsibilities
Computer literate; Proficient Microsoft Office skills including Word, Excel, and Outlook. Ability to adapt to multiple technology platforms/systems
Experience leading/supervising clinical research projects, including managing teams and the ability to prioritize, plan, delegate & evaluate deliverables; is well organized and structured, strong attention to detail
Clinical trial professional certification, e.g. CCRP, CCRA or CCRN
Experience interfacing with Regulatory Agencies such as FDA, European competent authorities & notified bodies, Health Canada, SFDA, KFDA, MHLW, etc
Knowledge of Quality Management Systems
Demonstrated experience prioritizing conflicting demands from multiple business entities in an extremely fast paced environment
Demonstrated ability to work well
Excellent verbal and written communication and presentation skills with the ability to communicate business issues in English in an easy to understand manner

Senior Clinical Research Associate Resume Examples & Samples

Manage and have accountability for clinical operations activities for all clinical trials for Client and potentially full project management responsibility for 1 or more smaller clinical trials including but not limited to
Protocol authoring and CRF design/development
Site selection and start up activities
Management of clinical monitoring activities
Clinical document authoring including informed consent forms, monitoring tools, CRF completion instructions, investigator brochures, etc
Additional responsibilities include
Act as the primary contact person for the clinical sites and vendors
Manage study CRAs and monitoring activities (including co-monitoring)
Lead feasibility activities as needed
Assist with outsourcing services to vendors including preparation of request for proposals, analytical review and feedback on vendor proposals and statements of work and direct input into the recruitment and selection of vendors
Manage clinical site contracts and payments
Manage central IRB or Ethics Committee approvals at sites for trials
Liaise with clinical data management lead and/or the data management vendor, if applicable, to ensure quality data is produced for each clinical trial in accordance with the protocol, statistical analysis plan and ICH/GCP and other regulatory requirements
Responsible for monitoring and tracking clinical drug supplies at the study sites
Responsible for evaluating clinical site and vendor performance
Assist with regulatory IND/NDA submissions as needed Participate in clinical audits, lead the effort to track and collect missing or outdated documents or follow up on outcome of clinical audits
Ensure understanding of appropriate Client SOPs, ICH-GCP guidelines
Ensure studies and clinical project deliverables are performed with quality standards and in accordance with ICH/GCP and other regulatory requirements
Additional duties as assigned by Director, Clinical Projects or VP R&
Strong understanding of the clinical trials process and regulatory requirements
Proven track record of successfully managing clinical trial activities in a quality manner and within the projected timeline and budget
Able to lead and work within teams and networks with internal and external team members promoting collaboration, effective work procedures and effective communication among the team
Demonstrate conceptual, analytical and strategic thinking
Demonstrate effective problem solving
Able to understand the impact of technology on studies and to use and develop computer skills
Current GCP training
Previous site monitoring experience
CRA or project management assistance in a pharm/biotech company
Expert in MS Word, Excel, and PowerPoint required, MS Project experience a plus
Possess excellent English language written and verbal communication skills
Strong organizing and planning skills to work independently with efficiency and accuracy
Ability to travel up to 15%

Clinical Research Associate Resume Examples & Samples

Clinical Research responsibility for marketed products, product modifications and/or assigned New Product Introduction (NPI)
Coordination of safety plans with Corporate Toxicology and scheduling of biocompatibility testing
Supporting Product Development Lab with In House Clinical Study (ICS) screening and verification testing during development
Conduct study site feasibility assessments and qualification visits
Bachelor's degree or higher in a Science or Engineering discipline from an accredited institution
Minimum of two (2) years clinical research experience
Bachelor’s degree or higher in Science, Nursing, Clinical Research or related discipline from an accredited institution
Certifications that include
Association of Clinical Research Professionals (ACRP, Certified Clinical Research Associate (CCRA) and/or
Society of Clinical Research Professionals (SOCRA), Clinical Research Professional (CRP)
Experience in one or more of the following areas: vascular access research, wound care research and/or skin research
Experience and knowledge of International Conference on Harmonization (ICH), Good Clinical Practice (GCP) and Food and Drug Administration (FDA) guidelines
Knowledge and experience with regulatory function
Experience in new product development programs

Clinical Research Associate Resume Examples & Samples

Completion of an allied health degree in clinical research. Associates degree in Clinical Trials Research related curriculum plus a minimum of eight years’ research experience (oncology preferred) or
Completion of a bachelor's degree plus a minimum of three years closely related research experience (oncology preferred) or
Completion of a master's degree in a health related field with four years directly related clinical trials research experience
Certification/license to practice as a Registered Nurse in North Carolina preferred. If not licensed, must be eligible for licensure/certification, other certifications as appropriate
Monitoring experience
Knowledge of the ICH guidelines, Good Clinical Practice (GCP ) DHHS, and FDA regulations
Experience in clinical research and regulatory processes and functions required
Experience in oncology preferred
Highly organized with attention to detail and knowledge of scientific, medical, and regulatory terms
Computer literacy, particularly in report design
A person with research experience at Duke Medicine or another academic-based health care delivery system with knowledge of clinical practice and research standards in a network setting
Clinical experience including but not limited to Nursing/patient care experience
Clinical Research Background*
Clinical Trials Monitoring Background*
Patient care experience*
= strongly preferred

Clinical Research Associate Resume Examples & Samples

Oversee and review routine and moderately complex site activities, withminimal tono guidance,through monitoring activities, including on-site visits and/or in-houseassessments, includingtelephone contact, and other technologies according to thetrial-specific monitoring plan to assessprotocol, regulatory, and SOP compliance with some guidance from anexperiencedCRA or aclinicaltrial lead
Completion of an allied health degree (e.g., Respiratory Therapy,Radiologic Technology, Licensed Practical Nurse) or Associates degree inClinical Trials Research related curriculum plus a minimum offour yearshealthcare experience; or
Completion of a master's degree in Public Health,., HealthAdministration or a related area with. one year directly relatedclinical trials research experience; or
Completion of a bachelor's degree plus a Minimum of two yearsdirectly related experience in clinical trials research; or4. Completion of a bachelor's degree plus a minimum of three yearsclosely related research experience.**State of North Carolina license may be required.**

Clinical Research Associate Resume Examples & Samples

Completion of an allied health degree (e.g., Respiratory Therapy, Radiologic Technology, Licensed Practical Nurse) or Associates degree in Clinical Trials Research related curriculum plus a minimum of four years healthcare experience; or
Completion of a master's degree in Public Health,., Health Administration or a related area with. one year directly related clinical trials research experience; or
Completion of a bachelor's degree plus a Minimum of two years directly related experience in clinical trials research; or
Completion of a bachelor's degree plus a minimum of three years closely related research experience

Clinical Research Associate Resume Examples & Samples

Ensure compliance/closure of Regulatory and Quality requirements before approving Design Outputs/Program Deliverables
Lead continuous improvement activities by driving the implementation of process and product quality improvement initiatives
Masters degree in a science related field with a minimum of 3 years experience with clinical trials management within the healthcare industry or Bachelors degree with 4 years experience in monitoring clinical trials
Excellent prior knowledge of all aspects of the clinical trial process including planning, execution and reporting/publication of results
Proven communication skills, both written and verbal, at all levels of an organization
Must be willing to travel as required
Must be legally authorized to work in the United States full-time
Must be willing to work in our [city, state] facility full-time
Must submit application for employment through gecareers.com (or COS if internal) to be considered
Must be willing to take a drug test as part of the selection process
Must be willing to submit to a background investigation, including for example, verification of your past employment, criminal history, and educational background
Well organized and structured, attention to detail
Ability to work independently and systematically
Diplomatic, cooperative teamworker

Senior Clinical Research Associate Resume Examples & Samples

Designs, plans, conducts, and monitors clinical studies
Prepares clinical reports for inclusion in regulatory submissions (e.g., CE Mark, 510K) and to support clinical claims
Monitors clinical study compliance
Interfaces with investigators, ethics committees and company personnel
Plans and conducts clinical investigator meetings
Works to ensure rapid and timely approval of products and support of marketing claims
Manages CROs
Manages Clinical study budgets
Negotiates Clinical Contracts
Expected to train and mentor others
Serve in a project leadership role
Knowledge of relevant medical device regulatory requirements (e.g. 510k, PMA, CE)
Technical knowledge and skills in clinical trial management for relevant products
Works independently on routine tasks
Great level of experience in the Clinical Research field
Relevant Degree
Understanding of GCP
Understanding of Clinical Trial Management
Understanding of Diabetes (desirable)
Understanding of Medical Device Regulations (Desirable)
Committed to caring
Responsible to our communities
Ready to apply our knowledge and know-how
Unique in our background and experiences
The drivers of our own success
Passionate about doing what’s right

Clinical Research Associate Resume Examples & Samples

Ensures monitoring, monitoring report review/finalization, event reporting and all other monitoring commitments are performed in accordance with the study monitoring plan
Manages assigned clinical sites, partnering with field monitors and site staff to identify and escalate or resolve compliance issues, and escalation of site questions or needs
Participates in site start up activities as assigned
Supervises screening & enrollment at assigned clinical sites
Routinely reviews site compliance data and works to identify compliance risks and issues
Partners with field staff to develop a CAP to address non-compliance issues as appropriate
Manages the completion of assigned project specific deliverables
Participate in site close-out activities for assigned clinical sites
Partners with colleagues to ensure assigned sites are audit ready at all times
Conducts a thorough comparison (monitor) of case report forms against medical records on complex trials at multiple sites
Addresses non-compliance issues and trends at investigative site; develops, documents and implements a CAP as necessary
Conducts qualifications, initiation, interim and close out visits. Ensures all appropriate site staff are trained, have access to required electronic systems, and are informed of data collection, GCP, protocol and reporting requirements
Participates as an extended team member of the clinical study team including: participating in study-specific meetings, teleconferences and investigator meetings
Conducts device accountability at clinical sites
Conducts study specific training for new study coordinators
Ensures that all adverse events are identified and clearly documented during visits
Serves as a mentor and trainer of junior Field CRA staff
Identifies and Reports complaints
Identifies and ensures communication of the need for corrective action at clinical sites. Collaborates with colleagues and clinical sites to develop and execute corrective action plans
Ensures training is completed per the required timelines and project needs
Identifies process improvement opportunities. Independently proposes solutions/plans
Tracks internal process metrics data to measure performance
Bachelor’s Degree in Science or Healthcare Related Field, or an equivalent combination of experience and education
3+ years experience in clinical/scientific research, medical device experience
CRM Electrophysiology device study experience preferred
Candidate needs to reside in location within reasonable travel distance to the St Louis, MO region
Must be able to travel 50-75%

Clinical Research Associate Resume Examples & Samples

The Clinical Research Associate (CRA) monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), and study protocols. Reviews regulatory documents as required and prepares site visit reports
May be responsible for multiple projects and must work both independently and in a team environment
Participate in the study development and start-up process including reviewing protocols, designing and/or reviewing Case Report Forms (CRF), preparing Informed Consent Forms (ICF’s), developing study documents, organizing and presenting at investigator meetings, working with management on a monitoring strategy, and/or developing project-specific CRA training. S/he may participate in clinical training programs and maintain awareness of developments in the field of clinical research as needed
S/he may provide a benchmark of monitoring competence to inexperienced/less experienced colleagues
Prepares clinical documents, business correspondence, and procedural manuals
Maintain systems and process necessary to report trial status and activities; and to help ensure that quality, regulatory-compliant clinical projects are conducted on time and within budget
Depending upon the level of experience, may become involved, when required, in other areas of study management and staff training and contributes to the review of sponsor/client’s and/or FHI 360’s systems and procedures as appropriate
Bachelor's Degree or its International Equivalent - Education, Health, Behavioral, Life or Social Sciences, International Development, Human Development or Related Field; Master's degree preferred
Must currently be located in Francophone West Africa
French fluency required
Must have at least 1 year of clinical research experience

Clinical Research Associate Resume Examples & Samples

Advanced degree or its international equivalent preferred
Supervisory or management experience required
Global clinical research work required
Spanish and/or French language proficiency strongly preferred

Clinical Research Associate Resume Examples & Samples

The Clinical Research Associate (CRA)/Zonal Team Leader, monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), and study protocols
Reviews regulatory documents as required and prepares site visit reports
Participate in the study development and start-up process including reviewing protocols, designing and/or reviewing Case Report Forms (CRF), preparing Informed Consent Forms (ICF’s), developing study documents, organizing and presenting at investigator meetings, working with management on a monitoring strategy, and/or developing project-specific CRA training
S/he may participate in clinical training programs and maintain awareness of developments in the field of clinical research as needed
S/he may provide a benchmark of monitoring competence to inexperienced/less experienced colleagues. Prepares clinical documents, business correspondence, and procedural manuals. Maintain systems and process necessary to report trial status and activities; and to help ensure that quality, regulatory-compliant clinical projects are conducted on time and within budget. Depending upon the level of experience, may become involved, when required, in other areas of study management and staff training and contributes to the review of sponsor/client’s and/or FHI 360’s systems and procedures as appropriate

Clinical Research Associate Resume Examples & Samples

Educate patients about clinical research protocols, study requirements and expectations
Adhere to legal, professional and ethical codes with respect to confidentiality and privacy
Collaborate with other members of the research team to ensure consistent practice in patient care management
Monitor on-site study sites to meet with, assist and consult with study investigators
Recruit and schedule all study site personnel as required
Track the expenditures for all study-related activities, including supplies and equipment
Create study documents, including protocols and amendments thereof, consent forms, data collections forms
Provide inputs to final reports that document the research findings for human use protocols including, but not limited to those listed above

Clinical Research Associate Resume Examples & Samples

2-4 years of related experience in scientific research and analysis
Familiarity with clinical research methodology is required
1 or more years of experience in direct provision of vestibular testing; experience with equipment such as NeuroCom and Rotary Chair, as well as vestibular rehabilitation techniques
Prior experience with participant and/or patient interaction in a clinical setting
Ability to follow detailed instructions and standard operating procedures
Excellent communication skills (verbal and written) and analytical skills required
S/he must adhere to legal, professional and ethical codes with respect to confidentiality and privacy

Clinical Research Associate Resume Examples & Samples

Possession of a Bachelor’s degree from an accredited college/university in a field related to biomedical research, clinical trials and/or health or four (4) years related experience in lieu of degree
In addition to education requirements, a minimum of two (2) years of progressively responsible experience in biomedical research including a minimum of one (1) year directly related to overseeing multiple concurrent trials and monitoring studies at clinical sites
Minimum one (1) year of on-site clinical research monitoring of studies for a sponsor or CRO
Ability to work in a clinical research setting, both independently and within a team
Ability to prioritize multiple tasks/projects and accomplish goals in expected timelines
Ability to communicate effectively, verbally and in writing, with non-technical and technical staff
Knowledge of clinical trial fieldwork, monitoring concepts and practices, FDA regulations and International Conference on Harmonization/Good Clinical Practices (ICH/GCPs)
Must be detail-oriented with strong organizational skills
Knowledge of TrackWise or similar Clinical Trials Management Tracking Systems
Ability to travel up to 60% locally, domestically and possibly internationally
ACRP Certified CRA or SOCRA Certified Clinical Research Professional
Infectious diseases/influenza experience
Knowledge of Department of Health and Human Service (DHHS) regulations
Experience with the development of CRFs, eCRFs, manual of operations and study monitoring plans
Experience with database applications
Knowledge of conducting federally funded studies
Ability to read and/or speak French or Spanish

Clinical Research Associate Resume Examples & Samples

A minimum of a Bachelor’s Degree and/or RN Degree is required
A minimum of 3 years clinical monitoring and clinical operations experience within a pharmaceutical, biotechnology, or contract research organization is required
Must have in depth knowledge of the Code of Federal Regulations related to clinical research, ICH GCP guideline and other applicable regulations and practices is required
Working knowledge, understanding and application of principles, concepts and practices of clinical research, experimental design and statistical analysis is required

Clinical Research Associate Resume Examples & Samples

Communication - Maintains timely and effective communication among team members and site staff. Routinely anticipates/identifies potential issues and implements corrective actions independently. Keeps project leadership apprised of team issues, seeking guidance as needed. Demonstrates effective conflict resolution
Monitoring - Responsible for site management and site staff performance including: monitors all types of clinical trials; participates in all types of site visits; assures compliance with all protocol requirements; assures effective patient identification and recruitment plan is in place; assures timely reporting of Adverse Events (AEs)/Serious Adverse Events (SAEs) and protocol violations; ensures proper storage, dispensation, and accountability of all Investigational Product(s) and trial-related materials; regularly reviews the status of the contents of the site regulatory binder; exhibits effective time management skills; may perform training visits with less experienced CRAs; and may perform assessment of less experienced CRAs during the sign-off visits
Data Handling - Performs source data verification according to contractual requirements. Assures timely completion and submission of Case Report Forms according to Clinical Monitoring Plan and/or Data Management Plan. Assures timely and accurate completion of Data Clarification Forms. Proficient with multiple data capture systems/methodologies in course of monitoring. Performs clinical data listings reviews as needed
Reporting and Tracking - Completes and submits reports according to SOP/Works Instructions (WI) or Sponsor requirements requiring minimal revisions. Maintains awareness of key study performance indicators for own sites, e.g. Telephone Communications Reports, patient enrollment, and SAEs. Updates study and patient status information and serves as Clinical Trial Management System resource for Project Manager (PM)/Lead CRA. Tracks Investigator payments/milestones. Documents and tracks the resolution of all outstanding site-specific protocol-related issues from visit to visit
Administrative - Prepares for and attends Investigator meetings. May attend Customer and Business Development meetings. May present materials, as requested. Assists with the preparation of study start-up materials and tools, as requested. Attends clinical monitoring staff meetings, project team meetings, clinical committees, and clinical training sessions according to the project communication, monitoring, and/or training plans

Clinical Research Associate Resume Examples & Samples

Independent clinical monitoring experience
Extensive understanding of SOPs, WI, FDA, and local regulations as well as ICH GCP guidelines
Effective command of written and spoken English language

Clinical Research Associate Resume Examples & Samples

Communication - Maintains timely and effective communication among team members and site staff. Anticipates/indentifies potential issues
Regulatory Documentation - Assures compliance with local regulations, Code of Federal Regulations. (CFR)/International Conference of Harmonization (ICH) and GCP guidelines, and Company and Sponsor. SOPs. Maintains current regulatory documentation according to Essential Regulatory Document Guidelines. and Trial Master File (TMF) Plan. Participates in TMF and on-site audits as requested; may require guidance to. respond to findings. May be responsible for assisting with the submission of regulatory packages to ethics committees and/or competent authorities
Monitoring - Assumes responsibility for site management and site staff performance including: monitors all types of clinical trials; participates in all types of site visits; assures compliance with all protocol requirements;assures effective patient identification and recruitment plan is in place; assures timely reporting of Adverse Events (AEs)/Serious Adverse Events (SAEs) and protocol violations; ensures proper storage, dispensation, and accountability of all Investigational Product(s) and trial-related materials; and regularly reviews the status of the contents within the site regulatory binder
Data Handling - Performs source data verification according to contractual requirements. Assures timely completion and submission of Case Report Forms according to Clinical Monitoring Plan and/or Data Management Plan. Assures timely and accurate completion of Data Clarification Forms. Utilizes multiple data capture systems/methodologies in course of monitoring. Performs clinical data listings reviews as needed
Reporting and Tracking - Completes and submits visit reports according to SOP/Works Instructions (WI) requirements. Maintains awareness of key study performance indicators for own sites, e.g. Telephone Communications Reports, patient enrollment, and SAEs. Updates study and patient status information and serves as Clinical Trial Management System resource for Project Manager (PM)/Lead CRA. Tracks Investigator payments/milestones. Documents and tracks the resolution of all outstanding site-specific protocol-related issues from visit to visit
BA/BS degree in science/health care field or nursing degree or equivalent combined education and experience. Previous clinical or related research experience preferred. Basic understanding of SOPs, WIs, FDA, and local regulations as well as ICH GCP guidelines; basic knowledge of applicable therapeutic standards. Strong organizational, documentation, and interpersonal skills as well as a willingness to work within a team-oriented environment. Native fluency in Japanese language (speaking, reading and writing) and able to handle business level English

Clinical Research Associate Resume Examples & Samples

Ability to travel approximately 50% is required
3-4 years experience as a CRA in biotechnology, pharmaceutical industry or CRO
Experience in effectively managing multiple tasks and projects
Ability to self motivate and work independently to meet timelines
Delegates work appropriately
Independently develops study documents and processes
Demonstrated ability to monitor all visit types independently
Understands the needs of stakeholders and able to develop action plans
Discerns urgency of issues and takes appropriate action
Good working knowledge of ICH & GCP
Responsible for the conduct and management of post marketing commitment studies, focusing in the areas of protocol development, study planning and implementation, site monitoring and management, enrollment and data quality
Responsible for feasibility assessments for new studies
Manages TMF contents and responsible for TMF reconciliation
Responsible for the preparation of study documents (i.e., consent forms, site instructions, etc.)
Responsible for the preparation of study training and investigator meeting materials and presents at study training workshops and investigator meetings
Responsible for the development and preparation of study startup, maintenance, and closeout activities, including monitoring plan
Responsible for the adherence to timelines, study quality and SOPs for assigned studies
Coordinate and complete all operational activities required for the registry startup, ongoing maintenance, and closeout of Medical Affairs (MAF) registry programs
Monitoring of registry programs at sites according to the monitoring plan
Participate in the selection of CROs and other vendors as needed
Responsible for the preparing reports that outline registry progress for both internal and external customers
Partner with the MAF team members to anticipate/identify potential problems with registry activities and develop and implement corrective actions to ensure success with these activities
Guidance of registry specialist activities supporting MAF programs

Senior Clinical Research Associate Resume Examples & Samples

Assist in the planning and execution of clinical studies ensuring that deliverables are completed on time and within budget
Create and manage reports that detail the clinical study progress such as subject screening and enrollment, data collection, documentation of adverse events, and payments
Assist with the development and management of study-related documents and materials such as investigational plans, case report forms, study manuals, monitoring plan, informed consents, websites, recruitment materials and other study related tools
Participate in site qualification and site initiation process, including review of required site documentation
Maintain current working knowledge of the disease state & product
Assist in training of investigators and coordinators
Assist with the development and implementation of site corrective actions as needed to address any noncompliance issues
Help with development and oversight of clinical database for the trial
May assist clinical manager by providing input to sections of clinical reports for FDA (510(K), IDE/PMA) and abstracts/manuscripts
Management of investigative sites to ensure sponsor support of trial activities and oversight of site compliance
Coordinate and conduct monitoring visits at participating centers to ensure compliance to the investigational plans, regulations, and timely receipt of data, including source document verification, device accountability, and writing of monitoring visit reports
Participate in regular project team meetings
Minimum of 5+ years experience directly supporting Clinical Research
Strong computer skills with a proficiency with MS Windows based applications
Strong organizational skills and able to manage multiple tasks

Clinical Research Associate Resume Examples & Samples

BS / BA in a related scientific or clinical field required
Minimum of 3 years related medical device / pharmaceutical field monitoring required
Field-based position and ability and willingness to travel up to 75%
Excellent interpersonal, problem solving and communication skills
Excellent follow-through capability
Self-motivated, attention to detail and organizational skills
Experience with various computer systems / applications and clinical trial management systems an willingness to learn new systems / databases

Clinical Research Associate Resume Examples & Samples

Ability to autonomously prioritize workload to meet study timelines while monitoring multiple protocols
Perform monitoring visits: Qualify potential investigative site, Train and initiate investigative sites, Conduct routine monitoring visits and close out visits
Complete on-time and thorough monitoring trip reports Review case report forms to ensure data compliance
Account for investigational devices ensuring the devices are available, stored appropriately, and accurately inventoried and documented
Verify appropriate reporting and documentation of adverse events and protocol deviations per protocol requirements
Ensure site regulatory binder is current
Manage investigative sites from study start up through close out
Provide support to the investigator evaluation and recruitment process
Create telephone scripts, feasibility questionnaires, and / or other related assessment tools for use in site evaluation
Assist in the collection of initial regulatory documentation
Assist in the preparation of study binders, manuals, or other site specific tools
Assist in the review of draft protocols, CRFs, and CRF Completion Instructions
Assists in the creation and / or revision of Clinical Affairs Standards and Work Instructions
Develop study specific monitoring tools
Perform study tracking activities as requested
Assist in Development of Clinical Monitoring Plan and / or other study related documents
Contribute to internal CRA meetings
Proactively identify issues which may interfere with study progress and implement strategies to resolve issues
BS / BA in a related scientific area Basic knowledge of clinical trial methodology relating to the monitoring of clinical trials, GCP, FDA, and / or country specific regulatory environment Minimum of 3-6 years of field monitoring experience Medical device experience preferred, but not required Proficient in MS Office Suite of products Experience with Clinical Trial Management System preferred Experience with EDC system preferred Excellent interpersonal and communication skills

Clinical Research Associate Resume Examples & Samples

Conduct training of investigators and coordinators
Coordinate and conduct monitoring visits at investigative sites to ensure compliance to the investigational plans, regulations, and timely receipt of data, including source document verification, device accountability, and writing of monitoring visit reports
Verify appropriate reporting and documentation of adverse events and protocol deviations per investigational plan requirements
Assist in planning, preparing, and presenting materials for investigator and coordinator meetings
Assist with vendor management to ensure that deliverables are completed on-time, within budget, and are consistent with the scope of work
Develop and maintain current working knowledge of the disease state & product
BA/BS or equivalent medical / industry experience
Minimum of 2+ years experience directly supporting Clinical Research
Strong working knowledge of Good Clinical Practices (GCP), FDA regulations, ISO 14155, and current industry practices related to the conduct of clinical trials
Previous experience with peripheral vascular devices preferred
Previous experience with EDC systems preferred
Ability to work effectively on cross-functional teams preferred
Valid driver’s license required
Able to travel 20% on average and up to 50% during peak periods

Senior Clinical Research Associate Resume Examples & Samples

Assist clinical team with study start-up activities
Thorough understanding of operational aspects of clinical research and regulatory requirements
Good interpersonal, problem solving and communication skills
Self-motivated, attention to detail and organizational skill
Experience with various computer systems / applications and clinical trial management systems; willingness to learn new systems / databases
BS/ BA or higher in a related scientific area preferred; a minimum of an RN is required
Minimum of 3 years related device / pharmaceutical field monitoring

Senior Clinical Research Associate Resume Examples & Samples

Serve as a leader and mentor to other CRAs in all aspects of the CRA role. May represent Regional Associate Directors and region at management meetings or other meetings as assigned and participate in decisions made at assigned meetings (e.g. site selection, site issue resolution). May interview prospective CRA candidates and assist with performance evaluation and management of CRAs
Ensure the site Investigator Folder is up to date and mirrors the Novartis TMF. Responsible for collecting regulatory documents from site and filing in the Novartis Trial Master File. Prepare and collect study site documents
Perform Initiation Visit and continue to train study personnel as needed on study protocol, procedures, study drug handling and storage, CRF (or eCRF) completion, SAE reporting, GCP, and possibly the drug mechanism
Responsible for utilizing and updating electronic systems to perform job functions (e.g. Outlook, WinFx, ClinTransfer, IMPACT, IWS, eTrial Master File webEDI, I.MAN, STARS, Vantage, SSU Database, Investigator Portal, LMS, ESOPs, iLearn, Expense reimbursement, CWT Horizon, Metrixx, Timecard, PMP, multiple eCRF applications). Serve as a reference to other CRAs on electronic systems. May be responsible for assisting with the evaluation, design and implementation of new systems
Ensure that study milestones are met as planned (i.e. database analyses, study startup, recruitment, closeout, etc.)
Prepare study monitoring reports, per Standard Operation Procedures (SOPs) and applicable regulations. May review and approve monitoring reports of junior CRAs as assigned
Manage data query resolution process with sites and track status updates (i.e. IWS)
Perform Site Closeout activities per SOPs and applicable regulations
Travel domestically (and possibly internationally) as needed to study sites and for training and meetings. A minimum of 50% overnight travel may be required
Attend and participate in disease indication and project specific training and general CRA training as required

Clinical Research Associate Resume Examples & Samples

Assist in and participate, plan, and lead study training meetings (e.g., investigator/coordinator meetings)
Assist study site staff, investigators, sales representatives, and other staff members regarding investigational products and protocol
Cardiovascular device trials
Cath lab, operating room and/or intensive care unit familiarity
Effective strategic, critical thinking, problem solving skills
Knowledge of computerized databases for the maintenance of scientific data

Clinical Research Associate Resume Examples & Samples

Ensure that all data and data collection from clinical research are handled according to applicable regulations and guidelines
Maintain dedicated investigation files to audit and inspection standards
Write protocols, amendments, case record forms, clinical reports and other documents relevant for dedicated clinical investigations. This includes ensuring the submission processes (CA + EC/IRB)
Ensure that monitoring is performed as planned including start-up and close-out meetings securing a quick start, good quality and adherence to timelines
Accountable for the handling of contracts and agreements with investigators, CROs, hospitals and universities
Accountable for the preparation, updates and adherence to budget including invoices/payment in dedicated investigations
Participate actively in preparing posters, abstracts and manuscripts
Coordinate with internal and external stakeholders to bring the investigation from "A to Z" according to plan and budget
Prepare and conduct or ensure relevant training for involved people including investigators, nurses, CRAs and other persons within Dentsply Sirona
Take part and initiate processes, procedures etc. in order to further develop the skills and capacity of the clinical research team

Clinical Research Associate Resume Examples & Samples

3+ years clinical study experience in medical device of pharmaceutical field
Working knowledge of Good Clinical Practice (GCP) guidelines
Proficient in MS Word, Excel, PowerPoint
6 months + experience with Clinical monitoring procedures
Ability to follow U.S. FDA and international regulations pertaining to medical devices and industry guidelines related to regulatory submissions, institutional review boards, clinical investigations, monitoring procedures and medical device reporting
Ability to travel as needed (25%)

Clinical Research Associate Resume Examples & Samples

Prepare and execute large scale (100 subject plus) external R&D verification trials –documentation, site training, IRB submission
Serve as primary contact for external sites and CRO for all study related questions
Monitor EDC production site for open queries and assist external sites in closing them with guidance from EDC programmer
Prepare and organize study materials, such as CRF’s and Informed Consent documents
Prepare and present training material for external sites
Create and submit IRB submissions and close out reports
Review and understand study protocol and ensure accurate execution of study procedure
Recruit, screen and schedule study patients via e-mail and phone
Directly interact with patients in the exam room: obtain informed consent, educate patient on study procedure
Assist as necessary in study methodology
Collect and enter study data on electronic data capture system and on paper
Compile and validate all study data
Reconcile study materials
Ensure accurate documentation following GCP and GDP
Maintain calibration, organization and cleanliness of the research clinic and exam rooms
Conduct monthly payroll run with EDC programmer and create purchase orders when needed
Perform monthly reclass report and quarterly Sunshine Act report
Study tracking and monthly reporting
Update and maintain patient database
Create and update SOP’s
Update and maintain research clinic website
Organize efforts and initiatives to attract new patients
Associate’s Degree /or Equivalent Education/Training
PC Skills (Microsoft Office Proficiency in the following: Outlook, Word, Excel and Internet Explorer)
Customer service orientedPreferred Qualifications
Microsoft Office Proficiency Access and PowerPoint
Experience in a Clinical research-focused environment
Health-related training and/or experience
Administrative support background

Senior Clinical Research Associate Resume Examples & Samples

Acquires a basic understanding of the principles of the assay and/or instrument and “hands-on” knowledge and skills in performing assigned assays or operating instruments
Serves as a consultant in a select area of expertise
Obtains and reviews all required essential documents necessary for study initiation
Conducts pre-study; initiation; interim; and close-out monitoring site visits and completes site visit reports
Maintains accurate and timely sponsor/site correspondence and communication
Prepares and presents project progress reports to keep management and team informed
Prepares standard the clinical sections of regulatory submissions and international registration packages
Coordinates preparation of responses to regulatory agencies’ questions regarding the clinical study
Prepares publications; abstracts; or presentations for professional meetings with minimal assistance
May advises and trains newly hired CRAs and direct others in the completion of tasks and projects
Maintains professional; product; and market expertise via independent reading; networking; and training
Volunteers for task forces; manages projects; or serves as a group leader. Encourages collaborative behavior; delegates effectively; and empowers others to take action. Gives effective feedback. Acts with fairness. Actions and words are congruent

Clinical Research Associate Resume Examples & Samples

Be primary point of contact for sites
Build and maintain relationship with sites
Monitor sites (Initiation Visits, Routine Visits, Close Out Visits, etc)
Produce monitoring reports within SOP and monitoring plan timelines
Coach investigators to be compliant with GCPs and the protocol
Talk to site staff about site recruitment
Ensure sufficient drug supply on site and reconcile drug on site
Ensure high quality data and conduct at sites
Identify and escalate issues or concerns to the internal Amicus team
Identify, analyze problems and trends; provide and recommend solutions across studies
Acts as liaison between CRO CRAs, Field Based CRAs and the PM
Accountable for reviewing and approving all trip reports for assigned studies
Develop training tools and training materials in support of the project
Develop study tools for sites and CRA use
Ensure that monitoring visits are performed in accordance with protocol/SOP monitoring plan requirements and that these are tracked, including report status and sign off
Accountable for the quality of the trip report content
Facilitate the review and provide input to the Monitoring Guidelines
Co-monitor with 3rd party CRAs as needed

Senior Clinical Research Associate Resume Examples & Samples

Lead the day to day support of study operations including tracking and creating overviews of subject, site, study status, milestones and performing quality check activities across components of the clinical study
Conduct and/or oversee clinical monitoring (site qualification, site initiation, interim monitoring, study closeout visits) activities to assure integrity of clinical data with respect to accuracy, accountability and documentation through review of case report forms, source documents, and medical records. May included monitoring visit report review and/or participating in co-monitoring visits
Assist in study set-up including but not limited to eCRF design, protocol preparation, informed consents, investigator selection, systems (e.g., CTMS), study related operational manuals, training materials, and various study plans (e.g., visit logs, monitoring plan, etc.)
Process and track clinical trial materials requests, study related supply requests, safety letters, vendor and investigator payments and other study related activities as needed
Collaborate with cross-function study team members to ensure compliance of department/study activities with FDA regulations, guidelines, and principles of ICH GCP and AIRM SOPs
Ensure complete and timely collection and archiving of TMF documents of assigned studies or program, including oversight and. or submission of regulatory documents to the TMF and ongoing document reconciliation
Assist in maintaining accurate and up to date study information within CTMS and other relevant tracking systems
Effectively communicate with study team members and work closely with Lead Study Manager to address challenges
May participate in process improvement and quality-related initiatives associated with study execution and deliverables
Responsible for complying with regulations and guidelines and ensuring adherence to these during study conduct
Travel Required: up to 25%
BA/BS with 4-8 years clinical research experience, or MA/MS with 2-6 years clinical research experience
Ability to work independently under general direction in a fast-paced environment
Minimum of 2 years prior clinical monitoring experience
Must have excellent interpersonal, written, verbal, presentation, administrative and computer skills
Moderate (25%) travel required

Senior Clinical Research Associate Resume Examples & Samples

Serve as clinical contact for a study including CROs/vendors, Investigators and study coordinators
Support the Clinical Study Manager and/or Director of Clinical Research with vendor selection and vendor management, including the Contract Research Organization (“CRO”) and other clinical study vendors (Central Lab, IVRS, Scale Management, etc.)
In conjunction with the Clinical Study Manager and/or Director of Clinical Research, manage site selection process for clinical studies
Assist and support development and review of clinical protocols, informed consent forms, or other study-related clinical documents (e.g. Case Report Forms, Source Documents, Monitoring Plan, Data Management Plan, Project Management Plan, etc.)
May accompany CRO/CRA’s to monitor activities at clinical study sites to assure adherence to Good Clinical Practices (GCP’s), SOP’s and study protocols
Assist in management and oversight of CRO in terms of the approved study budget and compliance to SOPs, and CRO personnel in terms of performance including selection and termination
Order and coordinate study supplies for clinical studies
Assist in review of vendor contracts and budgets
Assist and support data validation and data clean procedures
Assure regulatory compliance of investigational sites with SOP's and FDA and ICH
Minimum of 8+ years of experience in the pharmaceutical / biotechnology industry performing as a Clinical Research Associate with a combination of experience in in-house study management from study start-up to database lock, as well as, clinical site monitoring experience
Strong, relevant therapeutic experience in pharmaceutical/biotechnology clinical trials
Experience in selection and management of vendors/CROs (Central Lab, IVRS, EDC); previous experience as a Lead CRA or Clinical Team Lead is highly preferred
Experience in leading and working within functional teams
Ability to handle and prioritize multiple studies and projects
Ability to work effectively in a team/matrix environment
Ability to understand technical, scientific and medical information
Demonstrated strengths in planning, organizational, project management, analytical skills, oral and written communication, time management, conflict management, problem solving, attention to detail, and interpersonal skills
Ability to travel up to 25% travel including ground and air

Clinical Research Associate Resume Examples & Samples

7+ years of pharmaceutical development experience with at least 5 years of advanced site monitoring/management in complex small molecule and biologic trials in a wide array of diseases (oncology, transplant, HIV, etc.) across the development spectrum (phases I-IV, DMD, CRO partnership)
Mastery of all site monitoring visits (pre-post) while also understanding that site personnel may require support until lock
Extensive knowledge of ICH/FDA guidelines and thorough knowledge of global Health Authority (e.g., EMA, MHRA) regulations impacting activities in the US
Thorough knowledge, experience preferred, of industry trends (Risk Based Monitoring, Remote Monitoring, Remote Source Data Verification/Review, etc.)
Exhibits a high level of flexibility and sets an example for adaptability for changing priorities and processes
Employs strong fiscal management of departmental budget by independently managing travel and functional expenses
Demonstrates strong project management skills when engaging with stakeholders to ensure efficient management of timelines, resources, encountered challenges and stakeholders
Serves a role model for department through active planning, participation and representation on various projects, initiatives involving a wide breadth of internal and external stakeholders
Ability to manage successfully with designated book of work, adjust accordingly for risk based monitoring practices using critical thinking skills, and prioritize actionable items as necessary
1602518

Senior Clinical Research Associate Resume Examples & Samples

Investigative Site Monitoring - Demonstrate a commitment to quality in all aspects of monitoring; adhere to study monitoring plans; support site identification by conducting feasibility studies as needed; conduct Pre-study Visits for Investigative Sites; effectively facilitate/negotiate contracts for assigned sites within clinical subject budget as needed; conduct Study Initiation Visits at Investigative Sites; conduct Interim Monitoring Visits at Investigative Sites; review the investigator study file and reconcile versus the Trial Master File in compliance with GCP/ICH ; perform investigational product accountability and verify storage conditions; coordinate/organize the delivery of supplies as required; validate and track payments to assigned sites and patients travel reimbursement as needed; and conduct Close-out Visits at Investigative Sites
Data Integrity - Conduct Source Document Verification of CRFs against medical records to ensure CRFs are a valid representation of the subjects during their participation in a study; evaluate data query trends and interact with study team in order to improve data quality; assist investigative sites to achieve timely and accurate data entry and resolution of queries; ensure timely submission and review of CRF data and query resolution according to timelines set forth in the SMP; ensure issues of data quality are escalated and resolved/followed-up with the study team and CQA, as needed
Subject Safety - Monitor the informed consent process; perform safety reviews/SAE reconciliations; verify correct dispensing of IP to subjects; manage Investigative Sites’ adherence to GCP, ICH guidelines and local regulations
Train and Assist Investigative Sites - Attend Investigator Meetings, contribute and present when required; train investigative site personnel in GCP/ICH and study-specific requirements and monitor that sites are conducting Celgene clinical research according to the protocol, local regulatory requirements, and other appropriate regulations; serve as liaison between Celgene and assigned sites; build effective and positive relationships with site staff at assigned sites
Communication - Identify site issues, ensure proper escalation, if necessary, and ensure resolution/follow-up; create monitoring reports, confirmation/follow-up correspondence and telephone contacts for assigned sites; respond to audit findings if applicable; adhere to proper lines of communication within Celgene; attend and participate in study team meetings as assigned; keep information in the CTMS current; maintain calendar
Regulatory Documentation - Compile ethics submissions dossier in consultation with the investigator; support and ensure that country specific requirements are obtained when applicable; adapt patient information and consent form to local regulatory requirements to ensure approval; review translations for ICD and study documents as needed; ensure translation and back-translation of study specific documents as required; ensure local requirements are adhered to for EC updates (annual reports, protocol amendments and study completion/termination and safety reports where applicable); maintain local document files at a country level, as needed; liaise with Regulatory Affairs department for submission and any relevant change to be reported to a Competent Authority; maintain study information in the National Trial Database where appropriate
Development – Ensure that the medical and clinical knowledge for assigned therapeutic areas is up-to date with the support of line manager; develop and maintain a good working knowledge of relevant protocols; maintain a good working knowledge of FDA, GCP/ICH requirements and relevant regulatory requirements; mentor/coach new CRAs as needed; maintain annual qualification records
Examples of Monitoring Lead activities as required locally- serve on study team as monitoring Lead; review RFPs regarding monitoring specifications when required; develop study monitoring plan and subsequent revisions; review, track and acknowledge monitoring visit reports; manage and track monitoring site visits to ensure quality monitoring; highlight inadequate monitoring resources; track and report critical issues to study team; participate in CRF and protocol review process; conduct CRA/FM meetings
Others - Identify/evaluate potential investigators for future Celgene studies; participate and contribute to Clinical Research meetings, cross-functional activities and sharing best practices amongst the team as appropriate; contribute to adequate training of monitors in the study requirements; perform field assessments of Celgene and CRO CRAs, as required; develop study-specific tools for Investigative Sites and CRAs/Field Monitors; CRO monitoring oversight as required; create and review WPs and SOPs if applicable; identify study process improvements

Senior Clinical Research Associate Resume Examples & Samples

The contractor shall provide oversight and administrative efforts in order to efficiently and effectively monitor the clinical trial process
The contractor shall verify and ensure that the rights and well-being of the human subjects enrolled in the clinical trials are protected and that the reported trial data are accurate, complete, and verifiable from source documents
The contractor shall ensure that the conduct of the trial is in compliance with the currently approved protocol/amendment(s), with ICH current GCP, FDA CFR, USAMRMC, OTSG-DA, and DoD, along with other applicable Sponsor and regulatory requirements, requirements of host countries and other government regulations
The contractor shall lead the development, coordination, and implementation of monitoring and administrative strategies essential to the successful management of clinical trials research
The contractor shall conduct site pre-qualification and initiation visits; verifying that assigned research staff, facilities and investigational products have adequate qualifications and resources and these remain adequate throughout trials
The contractor shall conduct on-site clinical monitoring that includes; protocol training prior to study start, document reviewing, ensuring accurate data recording, monitoring adverse events, concomitant medications, and inter-current illnesses and verifies they are reported in accordance with the protocol on the Case Report Form (CRF), verify patient data, ensuring adherence to the clinical protocol, site and Sponsor SOPs, investigational product accountability, verification of product shipping/storage conditions, etc
The contractor shall conduct closeout site visits, including reviewing record retention requirements, investigational product reconciliation and securing and reviewing investigator’s final report
SCRAs must work effectively as part of an Integrated Product Team (IPT) and act as the Sponsor’s liaison to resolve site related issues quickly and effectively
The contractor shall prepare trip reports and recommend corrective actions, where appropriate, in accordance with USAMMDA SOPs
The contractor will maintain written or email communication as well as telephone communication with the clinical sites. Telephone communications will be documented in minutes
The contractor shall participate in reviewing protocols, amendments, investigator brochures, Informed Consent Forms (ICFs) and CRFs and facilitate Institutional Review Board (IRB) submission, queries, and approval
The contractor shall possess documented advanced training in GCPs as well as significant experience in clinical trial monitoring, including paper and Electronic Data Capture (EDC) studies
SCRA positions require travel 50-65% of the year
Maintain a safe workplace ensuring that he/she is aware of and observes appropriate safety and occupational health rules and regulations. Employee is required to attend safety training relative to his/her position and report any infractions of safety procedures to the facility Safety Officer
Must possess documented advanced training in GCPs as well as significant experience in clinical trial monitoring, including paper and Electronic Data Capture (EDC) studies
Possess a Bachelor's degree in Science/Health related field or equivalent experience
A Master's degree is preferred and will equate to 1-3 years experience
Shall possess 7-10 years in clinical trial monitoring
Certification as a Certified Clinical Research Profession (CCRP) or Certified Clinical Research Associate (CCRA) is preferred
SCRA positions may require travel up to 65% of the year
Must provide capability to learn, speak, write, and interpret foreign languages as appropriate
Must have the ability to obtain Secret Clearance

Clinical Research Associate Resume Examples & Samples

Support Clinical Trial Managers by coordinating necessary activities required for setting up investigational sites and monitoring a clinical study, completing accurate study status reports and maintaining study documentation
Update clinical trial management systems
Initiates, maintains and reconciles the sponsor study files in accordance with Standard Operating Procedures (SOPs)
Process site payments
Collects and reviews regulatory documents from clinical sites
Maintain tracking logs for departmental activities (i.e., training compliance, study related tasks)
Provide quality overview and consistency check on all developed ICFs and completes the informed consent checklist
3 year minimum administrative experience
3 or more years of administrative experience in a pharmaceutical or other health related industry, previous on-site monitoring experience preferred
Strong organization, time and self management skills
Knowledge of ICH/GCP guidelines
Ability to working in a team or independetly as required
Familiarity with Clinical Trial Management Systems

Clinical Research Associate Resume Examples & Samples

Regional location (US East Coast, Mid-West [Chicago, Atlanta, Philadelphia, New York City, Boston, Washington, DC, Charlotte)
At least four years of experience as a Clinical Research Associate. Experience in the management of multiple sites as a Clinical Research Associate is preferred
Excellent verbal and written communication skills, in addition to excellent organizational skills
Ability to travel 50% within North America is required
Monitoring: Ensures compliance of assigned sites with protocol, regulatory and overall study objectives. Confirms the qualifications of investigators, medical centers, and investigational sites throughout the conduct of a program and assesses adherence to Good Clinical Practice (GCP). Independently monitors clinical study sites: documents all findings, outcomes and agreements reached during site visits. Resolves discrepancies and ensures proper maintenance of site's documentation
Participates in co-monitoring visits
Participates in study meetings
Periodically reviews adverse events reported in the study and works with Pharmacovigiliance colleagues on reconciliation of safety databases. Oversees the required communication to the investigators as per the regulatory guidelines
Manages data discrepancies for assigned sties and coordinates the clinical monitoring activities to ensure that these discrepancies are resolved in the established timeframe for resolution
Manages laboratory specimen collection process where applicable including interfacing with laboratory and vendors. Ensures supplies for specimen collection are adequate at the site and site staff is trained on collection and shipment process
Identifies problems/issues and reports findings

Senior Clinical Research Associate Resume Examples & Samples

Minimum 1-2 years experience as a CRA or other related experience in the health care, biotechnology, diagnostics, or other relevant industry; related experience may include clinical trial assistant, project assistant, study assistant or study coordinator
Demonstrated competence with Microsoft tools, specifically Word; Excel; PowerPoint; and Project
Well-organized and detail oriented
Strong oral and written communicator with ability to maintain open communication with internal employees, managers and customers as needed

Senior Clinical Research Associate Resume Examples & Samples

Attend meetings with CRO and/or vendors and provide input during development or UAT phases
Assist in preparation and maintenance of ClinTrials.gov submissions
Comply with established company policies and procedures, objectives, quality assurance program, safety, and environmental standards
Attend seminars/conferences as required to keep up to date with clinical knowledge
Bachelor’s degree in a clinical or health related field, in life sciences, or equivalent work experience. Prefer RN or BSN

Senior Clinical Research Associate Resume Examples & Samples

3 years of onsite monitoring experience
Experienced in oncology/immunotherapy protocols
Strong understanding of ICH GCP Compliance
Ability to travel 65-70% of the month

Clinical Research Associate Resume Examples & Samples

Can conduct full range of data collection duties, including equipment setup and operations, execution of study per procedures, collect data, verify results and transfer data back to Masimo, etc
Plan, implement and conclude clinical studies in support of project timelines/market release goals with minimal supervision; An advanced individual may conduct more complicated studies, as well as contributes to study proposals and protocols, applying principles of clinical study design and research methodology to assigned research projects
Prepares and documents study plans, contracts, budgets, informed consents, IRB submissions, case report forms (CRFs), and other study related materials to assure quality, consistency, compliance, organization, storage and accuracy across all assigned projects
Contribute to clinical study design, proposals, protocols, etc., understanding basic scientific content, experimental design, and analytical approaches used
Can effectively work and communicate with investigator, staff and patients in professional, sensitive and mature manner
Conduct site monitoring (qualification, initiation, monitoring and close out visits) to insure and document site is trained to follow study procedures per protocol
Likewise, can monitor safety reviews and adverse event reporting for investigational medical devices to assure adherence to Good Clinical Practices (GCP), FDA and MDD regulations
Can suggest improvements to departmental procedures relating to GCP monitoring aspects
Can understands and operate Masimo products, data acquisition systems, following best practices for execution of study protocol and use of equipment
Insure essential study documents are properly organized and stored as quality records
Can conduct basic data analysis using spreadsheets, preparing basic calculations, statistics, graphs and tables
Writes clear, succinct and detailed clinical study and technical summary reports
Ability to travel extensively, perhaps 25-50% of the time, locally and domestically; Travel requirement is subject to change based on business needs
Must be able to lift and carry up to 20 pounds in order to: pack, ship, move, unpack, set up and execute equipment for study at clinical site, and then repack and ship back to Masimo
Perform special projects as requested
Experienced with Good Clinical Practice (GCP) in conduct of clinical studies
Excellent written and verbal communication skills essential
Must be capable of interacting with all levels of management, coworkers, investigators and subjects
Proficiency with Microsoft Office, computer data acquisition, data analysis, graphing and plotting results and report writing
Ability to independently set and manage multiple priorities
Demonstrates advanced judgment and decision making ability in the execution / oversight of clinical studies
Ability to travel to data collection sites, local and domestic, may require up to 25-50% of time
Ability to lift and carry up to 20 pounds
Experience with medical devices
Strong clinical background (e.g., respiratory therapy, nursing, pharmacology, physiology)
Excellent knowledge of FDA and ISO Good Clinical Practice (GCP) Regulations, Medical Device Directive, Canadian Medical Device Regulation, and other international requirements
Preferably certified as a Clinical Research Associate

Clinical Research Associate Resume Examples & Samples

Minimum of 3 years monitoring experience with at least 1 year experience of monitoring Oncology studies in the U.S.A
Excellent time management, project management, organizational, and communication skills (written and verbal) ) in local language and English
Expertise in and excellent working knowledge of core systems and tools
Preferred candidate will reside within the territory

Senior Clinical Research Associate Resume Examples & Samples

5 years monitoring experience with at least 3 years experience of monitoring Oncology studies in the U.S.A
Possess the ability to work independently and in a team environment
Excellent time management, project management, organizational, and communication skills (written and verbal) in local language and English
History of strong performance
Skills and judgment required to be a good steward/decision maker for the company
Possess an excellent working knowledge of all applicable ICH/GCP regulations
Preferred candidate will reside within the territory

Senior Clinical Research Associate Resume Examples & Samples

Manage clinical monitoring activities, including
Substantial monitoring experience in clinical research/Clinical Research Organizations
Solid understanding of therapeutic indications and study protocol
Ability to lead a "virtual" team
Competent in written and oral English and local language

Clinical Research Associate Resume Examples & Samples

Perform all clinical monitoring/site management activities for assigned projects in accordance with PAREXEL’s standard operating procedures
Act as PAREXEL’s direct contact with assigned clinical sites, and use judgment to assess and ensure overall integrity of study implementation, as well as adherence to study protocol
Minimum 2 years of monitoring experience in clinical research
Experience with CTMS preferred

Senior Clinical Research Associate Resume Examples & Samples

Arranging on-site visits and logistics
Establishment of a site recruitment plan in collaboration with site staff during QV
Performing site documentation verification
Data collection and drug accountability in accordance with ICH GCP guideline
Monitoring patient safety on-site and addressing any violations in a timely manner
Competent in written and oral English and Polish

Clinical Research Associate Resume Examples & Samples

Assist with development / review of study documents, which may include clinical trial protocols, ICFs, Case Report Forms (CRFs) and CRF Completion Guidelines, Clinical Monitoring Plan and Research Specimen Manuals
Assist with the review and analysis of clinical data for clinical trial report generation
Assess adequacy of potential clinical investigators and clinical trial sites. Includes evaluation of facilities, personnel, patient referral base, and adherence to GCP/ ICH
Act as one of the primary contacts between Seattle Genetics, Contract Research Organizations (CROs), vendors, and multiple clinical trial sites. Maintain close contact with clinical trial sites
Instruct clinical investigators and their personnel in regard to clinical trial protocol regulatory requirements, and with clinical trial specific training
Travel alone or with CRO representative to clinical trial sites to monitor compliance with the clinical trial protocol, CFR, GCP/ICH regulations, and overall protocol objectives
May act as Protocol Lead for small clinical trial, geographical region of large clinical trial, or close-out phase of any clinical trial study
May perform routine clinical trial site monitoring functions
BA/BS or equivalent or any relevant and qualifying training with a minimum of 4 years of relevant clinical trial management experience
Requires strong communication, interpersonal, and organizational skills
Knowledge of CFR and GCP/ICH requirements is required, as well as European Clinical Trial Directive is preferred
Must be willing to travel ( < 10 – 20%)

Clinical Research Associate Resume Examples & Samples

Serve as primary conduct for managing the relationship with assigned sites on behalf of UTC, cultivating productive relationships and understanding local challenges and opportunities
Conduct site evaluation, initiation, monitoring and close out visits
Develop and implement study specific monitoring tools
Conduct clinical site initiation visits, advise and train site personnel on sponsor and regulatory requirements for study conduct
Review on-site files and records, drug accountability, study supplies inventory, case report forms, and source documents for completeness, accuracy, consistency, and compliance; identifies deficiencies and discrepancies, and provide remedial training and/or initiate corrective action as required
Collect, review and process regulatory documents and correspondence from participating trial sites
Provide site support for remote / electronic data capture (EDC), review for completeness and consistency, and generate and resolve queries in between monitoring visits
Perform termination of clinical studies through resolving final queries and completing closeout visits
Regularly meet with PIs at assigned sites to keep them apprised of issues/concerns affecting the study
Gain a working knowledge of the diagnostic / therapeutic field and clinical trial material (CTM) that is to be studied
Provide support of CTM activities at site and study level. This may include study drug forecasting, assessing drug supply at clinical sites, reviewing and providing input on IVRS and drug accountability /reconciliation at clinical sites
Develop and implement recruitment plans to enhance site enrollment
Track personal finances for expense reporting and submission
Must be able to submit trip and expense reports in a timely manner

Senior Clinical Research Associate Resume Examples & Samples

Conduct site evaluation, initiation, monitoring and close‐out visits
Provide direction and training for other CRAs assigned to a project or study
Drive project success by working closely with CTLs to develop and implement enrollment strategies, monitoring and tracking tools
Provide quality accurate review of protocols and Informed Consent Forms (ICFs)
Review on‐site files and records, drug accountability, study supplies inventory, case report forms, and source documents for completeness, accuracy, consistency, and compliance; identifies deficiencies and discrepancies, and provide remedial training and/or initiate corrective action as required
Track subject enrollment and participation at each trial site
Maintain tracking tools to aid in monitoring, regulatory document review, and follow up of issue resolution. This may include maintaining site information on Clinical Trial Management System (CTMS)
Meet with PIs at assigned sites to keep them apprised of issues/concerns affecting the study
Respond to site’s questions about EDC use
Collaborate with CTL and CRA manager to respond to audit findings at the site level
Proficient in Microsoft Office (Word, Excel, PowerPoint)
EDC and CTMS experience preferred
Knowledge of regulatory and clinical practices (GCP, ICH)
Must be able to demonstrate aptitude and knowledge in relevant therapeutic areas and/or ability to learn and integrate new/different therapeutic areas
Must be detailed oriented, with strong time management and organization skills
Demonstrated ability to successfully perform all aspects of site management
Demonstrated understanding of relevant medical / therapeutic knowledge and medical terminology
Excellent understanding of Standard Operating Procedures (SOP) and Good Clinical Practices (GCP)
Strong interpersonal and written/oral communication skills
Understanding of the clinical research process, regulations pertaining to good clinical practice, and the requirements to successfully take a candidate drug through registration

Clinical Research Associate Resume Examples & Samples

Conduct Site Qualification, Initiation, Interim Monitoring, Close-Out visits and activities in accordance with FDA Code of Federal Regulations, Good Clinical Practice, guidelines, departmental procedures and the Clinical Monitoring Plan (CMP)
Ensures records are complete and consistent with governing regulations
Able to use or uses electronic data capture system and other monitoring tools to review and ensure accurate and complete clinical data collection
Assists sites with site-level IRB submissions, queries and documentation
Establishes and maintains regular communication with clinical sites
Conducts on-site interim site monitoring activities including document review, source data verification, informed consent forms, other site documentation and study material accountability
Prepare and complete monitoring visit reports and letters, and effectively document site communications Identify and address routine site issues including protocol deviations, subject recruitment and retention programs and communicate any observed study /data trends and proposed resolution
Resolves non-routine site issues in conjunction with the Study Lead
Assist with the development of clinical trial documents
Ensures distribution, collection, and tracking of regulatory documents to ensure site compliance and audit readiness
Assists in the validation and QC of clinical study database(s)
Provides input into the development of Clinical Monitoring Plan, informed consent forms, template source documents, study manual, regulatory binder and other study-related documents as needed
Advanced knowledge of clinical trial practices and regulations
Advanced knowledge of clinical monitoring and trial design
Proficient use of clinical trial databases
Proficient knowledge of technical computer systems
Willing to travel up to 50%
College Degree and minimum of 2-5 years of clinical monitoring experience

Clinical Research Associate Resume Examples & Samples

Project lead between the Mylan project team (PKDM Department, Product Development Department Chemistry Department, Quality Assurance Department, Mylan affiliate companies and various BD partners), clinical investigators and contract vendors for standard and complex bioequivalence studies
Site Manager for 3-4 Bioequivalence (BE) established and new CROs with responsibility to oversee all projects assigned to that CRO. Train new CROs and ensure established CROs are compliant with all study protocols, overall clinical objectives, FDA, ICH and other regional guidance and regulations, internal SOPs and Mylan departmental policies and SOPs. Maintain all required regulatory study documents, monitoring records and correspondence confidentially and in accordance with Mylan document control procedures for each project
Review all clinical and drug product documents for accuracy, completeness and timeliness internally and at the research sites. This includes review of Regulatory Documents, Drug Release/Accountability paperwork, Source Document templates, Case Report Form templates, Informed Consent Forms, Adverse Events, Dosing Logs, Protocol Deviations and Clinical Reports
Conduct clinical monitoring of studies remotely and on-site as required according to Mylan Standard Operating Procedures (SOPs). This includes visit preparation, monitoring process, completion of the monitoring report, visit follow-up activities and travel to and from the clinical locations
Interview clinical site research personnel in follow-up of monitoring visits and data issues. Communicate any substantial findings to his/her Supervisor during or immediately following a monitoring visit. Monitor and/or follow-up on the implementation of corrective action plans following clinical site inspections or audits, as required
Assist in management of patient trials and clinical endpoint CRO services related to site management and monitoring functions to include co-monitoring as needed
Minimum of a Bachelor's degree (or equivalent) and 2-4 years of experience in the field or related experience. However, a combination of experience and/or education will be taken into consideration
Certification (i.e., ACRP) as Clinical Research Associate preferred, but not required
Must possess knowledge of project management skills and pharmaceutical industry. Knowledge of and understanding of Good Clinical Practice and other associated regulations, guidelines and industry standards for clinical trials is required. Knowledge of medical terminology is desired
Must possess excellent oral and written communication skills. Good organization skills, attention to detail, ability to work as part of a team and the ability to manage multiple tasks is required. Must possess planning skills for a range of 6 months to 2 years in advance of study deadlines. Should be proficient in PC applications (Excel, Microsoft Word, etc.). Should have the ability to read and interpret documents. Ability to write routine reports and correspondence. The successful candidate must maintain a high level of professionalism and personal integrity
Ability to perform computations such as percentages, ratios, and rates. Ability to understand simple statistical analyses
Ability to solve problems with a variety of concrete variables through semi-standardized solutions that require some ingenuity and analysis. Ability to draw inferences and follow prescribed and detailed procedures to solve moderately complex problems
Ability to read and interpret complex business and/or technical documents. Ability to write comprehensive reports and detailed business correspondence. Ability to work with groups of people such as other departments and communicate known concepts. Ability to present to a group or department
30% travel is required to include extended international travel
Proficiency in speaking, comprehending, reading and writing English is preferred

Lead Clinical Research Associate Resume Examples & Samples

Perform all required tasks to ensure study execution under the supervision of the Manager Clinical Field Operations and Clinical Project Managers (CPM)
The Lead Clinical Research Associate (LCRA) coordinates and leads Clinical Research Associates (CRA) and sites in EMEAC assigned studies/registries for THV
The LCRA ensures that CRA activities are conducted in accordance with the internal quality system and external guidelines and regulations
LCRA ensures that the projects are conducted according to protocol and associated documents and that agreed study milestones and timelines will be achieved
The LCRA is responsible for the management of day-to-day aspects of study sites and CRA activities for the assigned projects and provides updates to the study team. As key member of the project team, the LCRA supports the development of the Monitoring plan and pays special attention to the adherence of the monitoring plan
A higher education degree in a scientific, health care, or other related discipline required
Minimum of 5 years field monitoring experience
Excellent knowledge of written and spoken English (and local language as applicable)
Expertise in communication, managing multiple priorities and computer literacy, supervisory and organizational skills
Desirable other European language
Understands and can apply knowledge of clinical trial designs to trial execution

Clinical Research Associate Resume Examples & Samples

40%: Study Start Up
Facilitate CDA & Contract Execution Process (Routing and tracking of study specific contracts)
Manage study specific PO Creation
Collaborate with Study Manager and CRO to ensure accurate study specific CTMS setup and data feeds
Liaise with Transparency group to ensure Clintrials.gov is updated accordingly
Participate in creation and distribution of sponsor specific study aides/materials and communications
Key point person for R&D select background checks
Collate documents required for the EC/IRB/HA submissions
20%: Study Maintenance
Assist Clinical Study Manager in tracking study related activities which are not appropriate to be outsourced
Agenda distribution & minute taking for internal study team meetings
Support SUSAR distribution
Maintain internal & external contacts lists in CTMS
Facilitate contract execution & study related PO creation for any change orders
25%: Departmental Tasks
Maintain knowledge and act as team super user for related systems (e.g. CTMS, R&D Select, PO creation, Sharepoint)
Maintain up to date training record attending internal/external training as necessary
Participate in inter-departmental workgroups to create or enhance processes
Take on career developmental activities/tasks as necessary
15%: Study Close Out
Assist study team with preparation for audits/inspections
Assist study team in close out in CTMS
Liaise with Transparency group to ensure Clintrials.gov and results are updated/distributed accordingly
Minimum 0-2 year's experience in relevant field (eg. Clinical Site, CRO, Sponsor or Clincal trial Vendor)

Clinical Research Associate Resume Examples & Samples

You should thrive in project teams and be focused on delivering exemplary levels of customer service
You will perform and coordinate all aspects of the clinical monitoring process
Effective oral and written communication skills, with the ability to communicate effectively with medical personnel

Clinical Research Associate Resume Examples & Samples

Clinical research experience in all phases of study life cycle, including start up, interim and close out
Equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities
Valid Driver's Licence
Valid Passport
Demonstrated performance management abilities
Extensive monitoring experience
Excellent judgment and decision making skills
Excellent interpersonal skills and problem solving ability
Ability to motivate and integrate teams and teach/mentor team members
Able to effectively prioritize workload
Knowledge of relevant regulations e.g. ICH/GCP, FDA guidelines, etc

Clinical Research Associate Resume Examples & Samples

A minimum of 18 months on site monitoring experience
In depth knowledge of ICH-GCP, EU and FDA requirements
Excellent English/Swedish language skills

Clinical Research Associate Resume Examples & Samples

Fluency in English and in the country's native language
Expert knowledge of FDA guidelines, GCPs and applicable Standard Operating Procedures
Skills to mentor and train other monitors in a positive and effective manner
Excellent team player with team building skills
Effective presentation skills

Senior Clinical Research Associate Resume Examples & Samples

Considerable clinical research monitoring experience (comparable to 5 years) with a demonstrated high level of expertise in all aspects of clinical monitoring
Expert clinical monitoring skills
Fluency in French, both written and spoken

Senior Clinical Research Associate Resume Examples & Samples

Independently performs monitoring visits, including Pre-Study, Study Site Initiation, routine Monitoring and Study Site Closure visits in accordance to GMCA SOPs and monitoring plan/conventions
Documents monitoring activities in monitoring reports and follow-up letters. Communicates serious issues to the study team in a timely manner
Serves as point of contact for investigators and site staff and maintains regular contact with study sites to ensure ICH-GCP/Regulatory/Protocol compliance, assessment of subject accrual rates and respond to sponsor/internal team prior, during and following site visits. Works with site personnel and study team to identify resolve and prevent issues
Oversees monitoring activities for a study to ensure the accurate reporting of high quality data and timely query resolution; ensure data is collected from sites within given timelines
Presents at and participates in Investigator Meetings, other study trainings and meetings as required
Ensures quality of data in the event that a site or CRA performance issue has been identified at a previously monitored site
Proactively prevents and identifies issues including study processes, monitoring or site issues
Develops clinical monitoring strategies for assuring study timelines are met and assuring quality deliverables
Develops the study Monitoring Plan and ensures CRA compliance with visit frequency and all assigned tasks throughout the study. Escalates CRA noncompliance to Study managers promptly
Reviews monitoring visit reports and assures adherence to study timelines for report submission and finalization
Oversees site start-up activities, including site selection and regulatory document collection, review, approval and tracking
Develops study specific CRA training materials. Trains CRA team and tracks and maintains documentation of training throughout the life of the project
Generates and utilizes metrics tools to assure study is running per timelines and to alert CRAs to potential issues (e.g., DM Query Trends, Missing CRF pages, Outstanding Monitoring Reports, etc.)
Works closely with CSM and other functional groups; collaborates with other departments as required and reports trial site status
Works closely with study managers for resourcing issues and to escalate pertinent CRA performance issues when necessary and provides feedback for annual appraisal
Assists sites in the preparation of IRB / IEC submissions
Works with CSM to manage vendors (e.g. Central Laboratory, CRF printers, Drug Distribution companies, etc.)
Works with CSM to assure investigator payments are appropriate and paid on a timely basis (if applicable). Works with CSM to oversee monitoring budget (control time spent onsite, reviewing monitoring reports to be billed on monthly basis)
Must have a strong understanding of Medical Terminology, Physiology and Pathophysiology
Must be highly organized and able to produce high quality work independently or as part of a team be able to multi-task and work in a high volume, deadline controlled environment
Must have an understanding of financial needs and processes (including Clinical budget), revenue forecasting / Recognition and invoicing practice
Must have excellent writing, verbal communication, interpersonal and diplomacy skills

Clinical Research Associate Resume Examples & Samples

Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Project Manager (CPM), Clinical Research Specialist (CRS) and/or line manager
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
Act as a mentor for new clinical staff
May provide assistance to the Clinical Project Manager and/or CRS with design of study tools, documents and processes

Clinical Research Associate Resume Examples & Samples

We are seeking enthusiastic and motivated individuals who want to stretch themselves in an environment that encourages learning
Able to work independently, you will enjoy communicating with others as you will meet a variety of healthcare professionals at monitoring sites, and interact with teams at Quintiles
Successful candidates will hold a Degree in a scientific or healthcare discipline and will have monitoring knowledge and strong expertise in a CRO or pharmaceutical environment
Experience in oncology is a plus
We also require the flexibility to travel up to 60% of the time
Fluent English Required (Oral and Written) as well as Computing Knowledge

Clinical Research Associate Resume Examples & Samples

Reviewing regulatory documents and preparing site visit reports
Participating in the study development and start-up processes
Reviewing and following study protocols
Designing and/or reviewing CRFs
Preparing informed consent forms and developing study documents
Organizing and presenting at investigator meetings
Working with management to develop project-specific CRA training
Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines
In depth therapeutic and protocol knowledge as provided in company training
Strong written and verbal communication skills in Norwegian including a good command of English language
Ability to establish and maintain effective working relationships with coworkers, managers and clients
Bachelor's degree in a health care or other scientific discipline
Over one year of on-site monitoring experience

Clinical Research Associate Resume Examples & Samples

Carry out assigned functions applying knowledge and skill in an accurate, timely manner
Perform specialized tasks as trained in an independent fashion, requiring minimal ongoing direction. Assist in the establishment of procedures and research methodologies
Monitor and maintain necessary supplies, with approval by senior department staff
Maintain records of activities and notebooks in a professional, accurate manner
Writes summary reports and supports protocol development
Travel to clinical sites for training, auditing, and closing clinical sites for Alere-sponsored clinical studies
Provide recommendations and observations to senior scientific staff on results of projects/tasks
Operate equipment and conduct tasks in a safe manner, adhering to established guidelines and applicable regulations
Interact with study coordinators at clinical sites to ensure optimal study progression and resolve problems
Accurately enter clinical data into a database and identify errors and discrepancies
Learn and apply knowledge of statistical methods to analyze clinical data
Knowledgeable of federal and other regulations, e.g. QSR’s, ISO, ISO 13485, CMDR
Carries out duties in compliance with established business policies
Perform other duties & projects as assigned

Clinical Research Associate Resume Examples & Samples

Conducting clinical monitoring visits, (ie, pre-study, initiation, interim and close-out) which includes all preparatory and follow-up aspects with a range of travel at 50-75% (approximately 10 days per month, e.g. for assigned site visits, investigator meetings, co-monitoring)
Trip report review
Attending weekly sponsor/project management teleconferences
Involvement in initial review of study documents
May present at Investigator's Meetings
Monitoring site performance and compliance and providing management with necessary reports, updates, and recommendations
Preparing clinical sites for regulatory agency audits
Assisting sites and data management with data query resolution

Clinical Research Associate Resume Examples & Samples

Works under general supervision, and participates in the design, planning, implementation and overall direction of clinical research projects; May coordinate the activities of relevant colleagues within the Company and investigators to ensure compliance with the overall scientific study objectives. May work with international investigators and key customers as well
Travels to field sites to monitor studies and provides technical assistance, when necessary
Receives general instructions; plans and prepares studies
Works with Data Management and Biostatistics staff on the design of documents and processes for the collection of study data from participating sites
Assumes responsibility for training and coordinating certification of study site personnel
Ensures accurate and complete study management/data collection and transfer to data management
Assists, prepares and manages study timelines
Conducts reference material testing in-house
Participates in Project Team Meetings
Keeps informed of trends and developments in clinical research
Knows and effectively uses the broad concepts of a particular field or specialization to resolve problems of limited scope and complexity
Analyzes alternative approaches to solve problems or develop new perspectives and existing solutions

Clinical Research Associate Resume Examples & Samples

Manage / Contribute to the study site selection process by preparing feasibility questionnaires and conducting site interviews
Organize investigator’s start-up meeting and study site initiation meetings
Develop various study specific forms/templates and prepares/ manages study status reports
Assist in vendor set-up, and oversight of vendors (including clinical CROs)
Review essential documents from study sites for accuracy and completion. Request set-up of TMF and review for reconciliation of required documentation
Be the first point of contact when investigators/site personnel enquire about patient inclusion/exclusion criteria for ongoing trials
Conduct monitoring visits and co-monitoring visits: coordinate with clinical investigators in the timely completion, submission, and review of CRFs and verify report data against protocol and patient files
Provide support to clinical investigators and study coordinators to resolve site-related issues
Communicate all relevant and critical issues to management
Assure compliance for assigned projects with clinical research policies and procedures
Manage progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
Contribute to the review of all SAEs, ensure Medical Director sign-off, site notification and compliance with all company procedures
Manage clinical aspects of database lock by participating in data listing review
Provide guidance to product supply process and oversee site shipments in alignment with the Clinical supply group
Contribute to clinical study design, proposals, and protocols
Contribute to patient recruitment strategies to increase patient randomization into the trial (e.g. investigator and research nurse meetings, newsletter updates)
Involvement in project follow-up (time planning, budget, project meetings) in collaboration with the CPM
Contribute to the Global Project Team for the assigned projects (Core team member)
Support junior CRA training
Contribute to the improvement of departmental procedures ( eg GCP monitoring aspects etc)
Comprehensive knowledge and understanding of Federal and International Guidelines as outlined in Title 21 of the Code of Federal Regulations, and ICH Guidelines of Good Clinical Practices required
Has ability to understand the disease under study and the aim of the therapy. Should be able to understand the relevant sections of the study protocol. Monitoring experience preferred
Has ability to maintain effectiveness under changing circumstances and priorities and must be able to handle multiple projects at a time and have strong attention to detail while keeping the global picture
Must be able to expand knowledge and adapt to an increasingly complex environment
Excellent verbal and written communication, presentation, interpersonal and organizational skills required and the ability to build effective relationships with site staff and colleagues
Proactive approach, tact and diplomacy strongly required
This position requires a sound knowledge of computer software and meticulous attention to detail
Must have experience in Electronic Data Capture (EDC) system
Should be process-oriented and should demonstrate a sense of urgency in completing deliverables through effective goal setting and a strong result orientation
Strong organization, documentation, and interpersonal skills
Ability to travel, including air travel, maintaining efficient and effective travel schedules, as the project could involve a lot of traveling, including overnight stays
Bachelor’s degree / Master’s degree in scientific discipline or equivalent
Minimum of 3-5 years clinical monitoring experience in a pharmaceutical, biotech, or medical device industry
Excellent command of spoken and written English / French. Other languages are a bonus

Clinical Research Associate Resume Examples & Samples

Assist in development of protocol, ICF, CRF, CRF completion guidelines, preparation and maintenance of monitoring plans, study binders, study manuals, and other site specific and monitoring tools
Request and collect initial regulatory documentation
Ensure that sites fulfill their regulatory obligations and submit study documents for IRB review and approval
Perform study tracking and reports progress in a timely manner
Plan and conduct training, site initiation, interim and close-out visits. Complete timely and accurate trip reports
Track and account for study devices; assess and monitor that investigational devices are available, appropriately used, handled correctly, stored, and accurately inventoried and documented
Monitor data and follow up with sites regarding timely completion and retrieval of CRFs and data correction forms
Assist sites to resolve regulatory document issues; ensure adequate study and regulatory documentation is maintained at the both the investigator site and Bard
Verify appropriate reporting and documentation of adverse device events, protocol deviations and subject enrollment
Communicate findings from contact reports and monitoring visits to Senior Manager and/or Project Manager in a timely manner
Initiate and track payments to study sites and external vendors as necessary
Experience in monitoring clinical study data and managing site-related issues
Knowledge of study protocols and case report forms, trial abstracts, and clinical publications
Attention to detail and organizational skill
Able to work with little supervision; must be a self-starter
Possesses working knowledge of computer/PC skills with experience in Microsoft Word, Excel, Access, Microsoft Project and PowerPoint, network systems (electronic mail) and Clinical Trial Management Systems

Clinical Research Associate Resume Examples & Samples

Minimum BS in scientific discipline or equivalent. At least 4 years related experience
Preferred: BA/BS/Nursing education and/or equivalent clinical research experience, preferably 3-5 years of clinical experience, e.g. CRA in pharmaceutical, biotechnology or medical device company including CRO. In Europe, degree in Biology, Chemistry or other life science, if less than 3 years clinical operations experience
Has familiarity with US Federal Food and Drug Administration, ICH/GCP/ISO, and European Regulatory Authority requirements, local regulations (e.g. JP) as applicable to a study
Demonstrated proficiency in computer operations in Windows® environment and is able to utilize available software for documents, spreadsheets and electronic mall
Must be able to handle multiple projects at a time and must focus on study specific needs while keeping the global picture
Excellent verbal and written communication skills required. Able to produce accurate and well-presented documents. Interpersonal and organizational skills are a must. Solution oriented mindset
Must be flexible in order to accommodate changes in team and project needs
Must enjoy working in global/international teams and be inclusive to others
This position is primarily sedentary work with the incumbent working in usual office working conditions with occasional walking/standing and lifting a maximum of 30 lb

Clinical Research Associate Resume Examples & Samples

Ability to prioritize workload to meet study timelines while monitoring multiple protocols
Work with the CRO and help provide documents to the clinical sites
Assist in Site qualification telephone calls
Assist in Development of Clinical Monitoring Plan and / or other study-related documents
Review and process monthly site payments
Initial review of AE’s and follow-up with CRO for necessary data for CEC meetings
Ability to travel up to 30% domestically
Basic knowledge of clinical trial methodology relating to the monitoring of clinical trials, GCP, FDA, and / or country specific regulatory environment
Minimum of 5 years of field monitoring experience
Medical device experience preferred
Proficient in MS Office Suite of products
Experience with Clinical Trial Management System preferred
Experience with EDC system preferred
Additional Desirable Qualifications Skills and Knowledge: Current Certification (CCRA) through ACRP
Current Certification (CCRA or CCRP) through ACRP or SOCRA

Clinical Research Associate Resume Examples & Samples

Independently responsible for all activities of the clinical trial including clinical site selection, study initiation visits, training of on-site personnel, study close-out visits and trial monitoring with on-site audits of clinical data for accuracy and completeness, and clinical report preparation and presentation
Identify potential investigators, prepare site budgets and contract agreements
Prepare study protocols investigator manuals, site specific instruction manuals and design case report forms for new and modified products
Assist with the management of key study parameters (i.e. trial master files, start-up activities, preparation of precision study specimens, data collection and data analysis, etc.)
Responsible for timely identification of problems or issues that could affect the results or timely completion of the trial, or any protocol deviations, and for suggesting mechanisms for solving the problem
Stay up to date on major advances in infectious disease diagnosis, cancer detection and the use of new tests and advances in clinical practice
The ideal candidate will have the following

Clinical Research Associate Resume Examples & Samples

Bachelor’s degree or its international equivalent in Health, Behavioral, Life or Social Sciences or other fields related to international/ human development. Master’s degree preferred
3 - 6 years of previous clinical research experience with at least 3 years being clinical monitoring experience
Articulate, professional and able to communicate in a clear, positive fashion with clients and staff
Must be able to read, write and speak fluent English and Spanish

Clinical Research Associate Resume Examples & Samples

Clinical Research responsibility for marketed products, product modifications, and/or assigned New Product Introduction (NPI)
Coordination of safety plans and scheduling of biocompatibility testing with Corporate Toxicology
Supporting the Product Development Lab by planning and conducting In House Clinical Studies (ICS)
Preparation of clinical protocols, study documentation and clinical reports as well as ongoing clinical study documentation requirements
Conduct study site feasibility and qualification assessments visits and monitoring visits throughout the conduct of assigned clinical studies
Development and maintenance of product claims sheets to support sales and marketing
Review and approval of marketing literature to ensure appropriate substantiation exists
Bachelor's degree or higher in a science or engineering discipline from an accredited institution
Minimum of one (1) year clinical research experience
Experience in one or more of the following areas: clinical study coordination, medical device or pharmaceutical development, infection prevention, oral care (dental), wound care research and/or skin research
Experience working in a hospital or clinical setting
Knowledge of Good Clinical Practice (GCP), International Conference on Harmonisation (ICH), and Food and Drug Administration (FDA) guidelines
Demonstrated experience in computer skills including Microsoft Word and Excel
Good organizational, IT, and administrative skills as the job involves a lot of documentation and recording of information through computerized processes

Clinical Research Associate Resume Examples & Samples

Possession of a Bachelor’s degree from an accredited college/university according to the Council for Higher Education Accreditation (CHEA) in a field related to biomedical research, clinical trials and/or health or four (4) years related experience in lieu of degree
A minimum of two (2) years of progressively responsible experience in biomedical research including a minimum of one (1) year directly related to overseeing multiple concurrent clinical trials and monitoring studies at clinical sites
Clinical monitoring/site management experience
Knowledge of clinical trial fieldwork, monitoring concepts and practices, FDA regulations and International Conference on Harmonization (ICH)/GCPs
Knowledge of Clinical Trials Management Tracking Systems
Familiarity with monitoring requirements to ensure integrity of data and site compliance as well as regulatory requirements and guidelines for clinical research
Mental health experience
Experience developing paper or electronic CRFs, manual of operations and study monitoring plans
Association of Clinical Research Professional (ACRP), Certified CRA or SOCRA Certified Clinical Research Professional (CRP)

Clinical Research Associate Resume Examples & Samples

0-2 years of related experience in scientific research and analysis
A minimum of 2 years specific training and/or experience completed or performed in Human Subjects Research preferred
Knowledge of the Health Insurance Portability and Accountability Act (HIPAA) and the ability to manage Protected Health Information (PHI)
Basic knowledge of Windows-based computer systems and applications to include Microsoft Word, Excel, and Outlook email
Must read, write, speak, and understand the English language fluently and maintain good communication skills with patients and other health care personnel
Possess experience with physiological data collection software

Clinical Research Associate Resume Examples & Samples

Regulatory Documentation - Assures compliance with local regulations, Code of Federal Regulations (CFR)/ International Conference of Harmonization (ICH) and GCP guidelines, and Company and Sponsor SOPs. Maintains current regulatory documentation according to Essential Regulatory Document Guidelines and Trial Master File (TMF) Plan. Participates in TMF and on-site audits as requested. Responds to findings without oversight. May be responsible for submission of regulatory packages to ethics committees and/or competent authorities
Monitoring - Responsible for site management and site staff performance including: monitors all types of clinical trials; participates in all types of site visits; assures compliance with all protocol requirements; assures effective patient identification and recruitment plan is in place; assures timely reporting of Adverse Events (AE)/Serious Adverse Events (SAE) and protocol violations; ensures proper storage, dispensation, and accountability of all Investigational Product(s) and trial-related materials; regularly reviews the status of the contents of the site regulatory binder; exhibits superior time management skills; may perform training visits with less experienced CRAs; and may perform assessment of less experienced CRAs during the sign-off visits
Data Handling - Performs source data verification according to contractual requirements. Assures timely completion and submission of Case Report Forms according to Clinical Monitoring Plan and/or Data Management Plan. Assures timely and accurate completion of Data Clarification Forms. Highly proficient with multiple data capture systems/methodologies in course of monitoring. Performs clinical data listings reviews as needed
Administrative - Prepares for and attends Investigator meetings. May attend Customer and Business Development meetings. May present materials, as requested. Assists with the preparation of study start-up materials and tools, as requested. Attends clinical monitoring staff meetings, project team meetings, clinical committees, and clinical training sessions according to the project communication, monitoring and/or training plans

Senior Clinical Research Associate Resume Examples & Samples

Perform Initiation Visit and continue to train study personnel as needed on study protocol, procedures, study drug handling and storage, CRF (or eCRF) completion, SAE re-porting, GCP, and possibly the drug mechanism
Conduct feasibility and screen potential Investigators and networks to evaluate their capabilities for conducting clinical trials. Nominate sites to participate in studies in con-junction with Medical Science Liaison (MSL) and Clinical Research Medical Advisor (CRMA) colleagues
Computer literacy and proficiency
Ability to multi-task and prioritize multiple high-priority projects, site questions, CRA questions, and clinical team inquiries while managing responsibilities and deadlines

Clinical Research Associate Resume Examples & Samples

Solid understanding of clinical development process including GCP and ICH guidelines
Proven ability to work on teams and deliver on commitments
Knowledge and experience in international (FDA, EMEA) and local regulations as well as Novartis stand-ards
At least 2 years experience as CRA

Lead Clinical Research Associate Resume Examples & Samples

Bachelor's degree required (Advanced degree or certification preferred but not required)
Minimum 5 years of experience in similar role (eg. Sponsor, CRO or Clinical Study Vendor)
In depth knowledge of operational start up activities for phase I-IV clinical studies
Ability to mentor peers to build on strengths/weaknesses and drive success
Relevant experience in clinical research or related field
General knowledge of regulatory requirements and guidelines governing clinical research
Comfortable with technology and ability to learn new systems quickly
Strong knowledge of MS Word, Excel, PowerPoint and Outlook
Requires strong attention to detail in composing and proofing materials, establishing priorities, scheduling, and meeting deadlines
Must be able to work in a fast paced environment with demonstrated ability to manage multiple competing tasks and demands
Understanding how their input and role coordinate more effective business practices for Shire’s Clinical Development business and commitment to the culture, vision, and mission of Shire
Ability to take ownership and manage tasks as well as communicate effectively
Ability to lead others to drive deliverables forward
Must be able to work in a fast paced environment
Demonstrate ability to prioritize multiple competing tasks
Ability to work with minimal supervision and complete tasks according to deadlines
Available for up to 10% domestic and/or international travel

Senior Clinical Research Associate Resume Examples & Samples

Prepare study monitoring reports, per Standard Operation Procedures (SOPs) and applicable regulations
Attend disease indication and project specific training and general CRA training as required. May participate in the training of other CRAs at meetings
Perform additional roles and functions for GenMed Clinical Operations as assigned such as a Trial Lead CRA, systems superuser, or committee member
Up to 2 years of prior experience in a clinical research role as either a CRA or site CRC or relevant experience
Demonstrated ability to coordinate, organize, communicate, and manage site activities, with knowledge of when to escalate issues to Management or Clinical Team

Senior Clinical Research Associate Resume Examples & Samples

Committee experience (CEC/DSMB/Steering)creating/leading independent physician committees
Experience managing a core lab (Imaging, Echo or CT)
Experience with putting processes into place (SOP, Charters, etc.)
Experience creating study documents
Enrollment experience

Clinical Research Associate Resume Examples & Samples

Review on-site files, product accountability logs, study supplies inventory, case report forms, and source documents for completeness, accuracy, consistency and compliance; identifies deficiencies and discrepancies and provides remedial training and/or corrective action as required
Develop and implement study specific tracking tools to aid in monitoring, regulatory document review, and follow up of issue resolution
Provide site support for remote/electronic data capture (EDC), review for completeness and consistency, and generate and resolve queries in between monitoring visits
Completion of monitoring reports and follow-up letters, which includes providing summaries of significant findings, deviations, deficiencies and recommended action to secure compliance
Ensure that studies adhere to FDA regulations, Good Clinical Practices, and IVD directives
Bachelor's degree in a scientific discipline (Clinical Sciences, Health/Life Sciences, Molecular Biology, Biochemistry and/or Human Physiology), RN or BSN degree or equivalent
Prefer 1-2 years of experience with In Vitro Diagnostic (IVD) products
Excellent communication and team skills
Proficient in Microsoft Office Applications, such as Word, Excel, Access, PowerPoint etc
Experience in the handling and shipping of Bio hazardous specimens
Must remain current with regulatory and clinical requirements for diagnostic products and translate the regulatory requirements into clinical trials
Knowledge of GCP & ICH guidelines and FDA regulations
Working knowledge of the diagnostic field and clinical trial material that is to be studied
30-50% travel required
Good understanding of medical terminology, human physiology and laboratory testing
Experience with laboratory automation and biological databases
Previous hands-on experience in clinical research at either a diagnostic company/hospital or laboratory
Knowledge of good clinical trial design, including the number and types of subjects and specimens that will be required, the conditions under which specimens must be collected, and the current gold standard for the diagnosis of disease

Clinical Research Associate Resume Examples & Samples

2+ years of previous pharmaceutical or medical device clinical study coordination, clinical site monitoring, or clinical study management experience required or equivalent combination of education and experience
Prior experience with current Good Clinical Practices (cGCP) and Code of Federal Regulations (CFR) preferred
A background in biomedical/healthcare services with laboratory experience preferred
Works within project teams to facilitate the conduct of standard study designs
Participates in clinical affairs meetings and completes independent activities to support departmental functions
Completes all internal training programs in a timely manner, and demonstrates professional development via independent reading, networking and training
Adopts clinical practices that promote Quality First Time
Excellent skills in basic computer applications (Word, Excel, Access, PowerPoint)
Well organized and detail oriented
Impeccable record keeping and filing skills
Ability to give presentations and teach others
Ability to work effectively in a team, and also work independently on assigned tasks
Ability to complete intermittent overnight travel up to 30%

Senior Clinical Research Associate Resume Examples & Samples

Ability to maintain customer focus through the utilization of good listening skills, attention to detail
Ability to remain flexible and adaptable in a wide range of scenarios
Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software
Monitors investigator sites to ensure the accuracy and validity of CRF entries in
Participates in investigator meetings as necessary. Identifies potential

Clinical Research Associate Resume Examples & Samples

Maintains required functional and job specific training
Moderate understanding of SOPs, WIs, FDA and local regulations as well as ICH-GCP guidelines
On site experience: signed off to independently conduct at least two types of visits; PSSV, SIV, IMV, COV
Experience of Observation/Training visit on all types of visits. Competent in independent drug accountability
Competent in independent investigator site file review
Demonstrates understanding of all Essential Documents and their collection and maintenance
Off-site experience: familiarity with basic category of Clinical Monitoring Associate tasks. Ability to understand/guide site staff to execute on clinical protocols
Understanding of local regulatory, safety, and GCP. Demonstrate proficiency in navigation within: CTMS systems, Data Platforms for projects, Microsoft Suite: Excel, Word, Power Point, Outlook, Site EMR systems
Model professional communication in both written and verbal interactions
Demonstrate sufficient time management to achieve required deliverables
Ability to handle multiple tasks to meet deadlines in a dynamic environment

Clinical Research Associate Resume Examples & Samples

Knowledge of clinical trial practices and regulations
Knowledge of clinical monitoring and trial design
College Degree and minimum of 1-2 years of clinical research experience. Monitoring experience is a plus

Senior Clinical Research Associate Resume Examples & Samples

80%
Provides clinical study start up expertise and ensures identified efficiencies within study start-up are implemented
Assists in providing oversight of site identification and selection
Provides oversight of Clinical CRO activities regarding Legal review/negotiation/execution of confidentiality and site agreements
Provides oversight of Clinical CRO activities regarding country and site specific informed consent documentation tracking, finalization and approval
Ensures effective communication between Shire and the Clinical CRO
10%
Maintains knowledge and act as team super user or subject matter expert for related systems and processes
Maintains up to date training record attending internal/external training(s) as necessary
At least 3-5 year's experience in similar/relevant job (eg.Sponsor, CRO, or Clincal Study Vendor)

100

Clinical Research Associate Resume Examples & Samples

Performing monitoring activities according to legislation requirements and Novo Nordisk SOPs
Submission on Clinical Trials Protocol and Amendments to HA and EC
Trial Site Initiation and Closure
Preparing recruitment strategy at country and site level in agreement with Clinical Trials timelines
Reporting of adverse events within the timelines given in local legislation/SOPs
Site selection
Contract preparation and negotiations
Managing trial material and ensuring site are provided with the amount needed in timely manner
Clinical Trial budgeting and monitoring of related expenses

101

Clinical Research Associate Resume Examples & Samples

Support the investigator evaluation and recruitment process
Perform essential document collection, quality control, review and tracking
Ensure that Bard and investigator obligations are being met and are in compliance with the study protocol, GCP-ICH Guidelines and applicable regulations
Support investigative sites in fulfilling their obligations with regard to submissions to local regulatory and IRB/IEC requirements
Perform study file audits to ensure that the study files are current, accurate and complete
Track clinical trial management metrics
Provide support to internal and external teams to meet project specific goals
Participate in project related meetings
Assist with investigational product accountability, subjects screening/enrollment, case report form retrieval, query distribution to/retrieval from investigative sites
Verify appropriate documentation and reporting of study events
As required by certain projects, provide support to resolve internal and external clinical issues
Assist in the creation and maintenance of clinical project documents, including project plans, monitoring guidelines, data management plans, site study manuals, monitoring visits reports, letter templates, study materials, template log forms and study presentations
Interact with investigative sites, vendors and other Bard functional areas as secondary project contact for clinical issues
Participate in site qualification and site initiation process, including scheduling of monitoring activities with site personnel
May coordinate and conduct monitoring visits at participating research sites to ensure compliance to the investigational plan, regulations and timely receipt of data, including source document verification, device accountability and writing of monitoring visit reports
Assist in training of Coordinators

102

Clinical Research Associate Resume Examples & Samples

Responsible for data monitoring and study site management
Work according to Good Clinical Practice, rules and regulations and internal procedures
Support site identification, selection, i.e. recruitment & qualification, and initiation
Assure study site management; conduct data and study site monitoring activities for clinical studies, assure investigators and study site personnel adhere to the study protocol, applicable local regulations, ICH/GCP guidelines and SOPs, monitor study progress, executes close out activities and authors related reports
Oversee and coordinate the work of third party CRAs (CRO-CRAs)
Support development of regulatory binders and investigational product shipments as applicable
Other activities as assigned
At least 2 years related experience in (conducting) clinical trials (healthcare setting , CRO, medical device and/or pharmaceutical company and/or industry)
A demonstrated working knowledge of GCP, ICH guidelines, FDA/EU regulations
Excellent record-keeping skills; good documentation practice
Ability to maintain excellent working relationships with a broad range of trial staff
Flexibility in work hours and readiness to travel

103

Senior Clinical Research Associate Resume Examples & Samples

Manages and oversees for the Bayer Consumer Health (BCH) Personal Care Franchise the operational conduct of all types of Consumer Research Studies (e.g. Sensory Testing, testing of Consumer Commodities or devices, Consumer Care Insight Tests / Consumer Tests) in humans in which a subject is physically exposed to a BCH product or active product ingredient from obtaining bids working with sourcing to final study report
Works closely with Clinical Trial Manager on the preparation and conduct including monitoring of safety, efficacy and claims studies for Personal Care products. This includes amongst others the receipt of necessary documentation for the Trial Master Files (TMF) as well as TMF maintenance, control of budget, communication with and to Clinical Research Organizations (CROs), Laboratories, and other external vendors involved in the conduct of studies. Collection and maintenance of submission documents, including EC/IRB submissions
Operational expert for the set-up, preparation and conduct of Sensory Testing, testing of Consumer Commodities, Consumer Care Insight Tests / Consumer Tests in humans in which a subject is physically exposed to a BCH product or active product ingredient
Ensure that all applicable guidances including, however not limited to ICH Guidelines, GCP and SOPs are followed in all aspects of the studies
Partner with CRO data management staff to process Case Report Form (CRF) and subject reported outcome questionnaire development
Operational activities for the execution of efficacy, safety and claims studies for Personal Care Products
Oversee administrative activities, maintenance of study documentation, collection and review of IRB/EC submissions
Coordinating ethical committees/independent review board (EC/IRB)
Perform study initiations, carry out interim monitoring visits with the timely completion of reports and oversee these activities conducted by internal and external CRAs and/or CROs
Ensure timely recruitment of subjects and smooth running of subsequent operations, including data flow
Account for and reconcile all used and unused trial supplies
Closing down or oversee closing down of study sites on completion of the trial including archiving study documentation and correspondence
Bachelor’s or (international equivalent) in Nursing, Life Sciences, Health Sciences or other scientific/health- related field. Minimum of four years of experience in clinical biomedical development, preferably with 2-3 years in the field of clinical trial monitoring as a CRA
Ability to work on-site in Morristown, NJ
Solid knowledge in in tracking clinical study costs against the budget
Knowledge of, and adherence to ICH/GCP Guidelines, and as well as appropriate guidelines for clinical monitoring are required
Knowledge and cross functional understanding of clinical trial methodology and logistics
Team player with ability to work independently to accomplish objectives within timelines established by the Clinical Trial Manager and /or Project Teams
Experience working in a matrix organization
Position requires willingness for business trips, up to 25%, partially with significant frequency
Excellent written and verbal communication skills, interpersonal and organizational skills are preferred

104

Senior Clinical Research Associate Resume Examples & Samples

Manage and oversee the Bayer Consumer Health (BCH) Personal Care Franchise the operational conduct of all types of Consumer Research Studies (e.g. Sensory Testing, testing of Consumer Commodities or devices, Consumer Care Insight Tests / Consumer Tests) in humans in which a subject is physically exposed to a BCH product or active product ingredient from obtaining bids working with sourcing to final study report
Operational activities for the execution of efficacy, safety and claims studies for Personal Care Products, Oversee administrative activities, maintenance of study documentation, collection and review of IRB/EC submissions
Ability to be On-Site in Morristown, NJ

105

Senior Clinical Research Associate Resume Examples & Samples

Experience in a pharmaceutical, biotech or CRO company
Minimum 2-3 years of Clinical research experience, ideally with Vaccines and or/Infectious diseases and/or Oncology
Management of regulatory and / or IEC questions

106

Clinical Research Associate Resume Examples & Samples

Conduct site pre-study, initiation, routine monitoring, and study closeout visits
Monitor, track, and manage all study related tasks at study sites ensuring compliance with GCP, ICH, applicable regulations and company SOPs
Collect, review, track, and ensure appropriate completion of site-specific study/essential documents. Performs ongoing reconciliation of the Trial Master File (TMF) content to site files
Primary contact for study site personnel
Provide training to site personnel
Track and report progress of study sites
Responsible for quality data from study sites. Ensures appropriate source documentation, training, and accurate transcription of data into the study Case Report Form (CRF) as evidenced by minimal data query rates. Ensures timely reconciliation of data queries and implementation of process improvement/corrective action when needed
May take meeting minutes, develop and maintain study trackers, or assume other tasks to support study team
Coordinate, assemble, and ship study related supplies as needed
Assist with creation and review of study tools/documents
Maintains awareness of overall development in the field of clinical research based on current literature, attendance at professional meetings, continuing education, etc
Requires a Bachelor’s degree (BA, BS or BSN) from a four-year college or university in a scientific discipline or equivalent combination of education and work experience plus minimum of two years pharmaceutical clinical research experience
Knowledge of GCP/FDA/ICH regulations required
Have a broad understanding of clinical research. Have a working knowledge of the relevant SOPs
Have the necessary interpersonal and communication skills to establish professional working relationships with colleagues and site personnel
Attention to detail and the ability to prioritize. Strong organizational, planning and follow-through skills
Ability to work well under pressure and with tight schedules
Ability to exercise judgment within generally defined practices and policies for obtaining data
Self-direction and motivation are mandatory
MS Word, Excel, in-depth knowledge of other presentation programs a plus
Must be available to work in the evenings and weekends, as required
Must have the quality-service attitude and be willing to work additional hours to meet deadlines

107

Clinical Research Associate Resume Examples & Samples

Participates in the design and monitoring of clinical trials
Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives
Performs a variety of complicated tasks
Typically reports to a supervisor or manager
Knowledge of FDA regulatory requirements is required
Familiar with a variety of the field's concepts, practices, and procedures in a clinical research setting

108

Clinical Research Associate Resume Examples & Samples

Participates in the design, administration and monitoring of clinical trials
Analyzes and evaluates clinical data gathered during research
Ensures compliance with protocol and overall clinical objectives
Relies on instructions and pre-established guidelines to perform the functions of the job
Works under immediate supervision
Primary job functions do not typically require exercising independent judgment
Knowledge of commonly-used concepts, practices, and procedures within a clinical research setting

109

Senior Clinical Research Associate Resume Examples & Samples

Bachelor's degree, typically in nursing or scientific field, or the equivalent
4+ years direct CRA experience in the pharmaceutical industry or equivalent in clinical study management
Ability to prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions and procedures
Possess excellent organizational skills
Ability to effectively communicate and interact with key contributors including but not limited to physicians and clinical staff and to communicate technical information both verbally and in writing
Ability to manage multiple tasks simultaneously

110

Clinical Research Associate Resume Examples & Samples

Bachelor degree or equivalent education/degree in life science/healthcare required if accompanied with 2 years' experience in clinical setting
2+ years of relevant clinical experience in a CRO or pharmaceutical industry
Excellent communication, organization and tracking skills
Strong operational skills and demonstrated ability to meet timelines
Proven ability to work both independently and in a team setting, including a matrix environment
Knowledge of Good Clinical Practice; thorough knowledge of clinical trial design; understanding of the overall drug development process

111

Clinical Research Associate Resume Examples & Samples

Evaluates and analyzes clinical data
Must have knowledge in reference to good clinical practices regulations and standard operating procedures
Coordinates activities of associates and investigators to ensure compliance with protocol and overall clinical objectives
Maintains a high level of professional expertise through familiarity with clinical literature and participates in project team meetings
May draft materials including informed consent documents, draft source documents, patient instruction guides and case report forms
Conducts clinical monitoring of field sites to supervise and coordinate clinical studies
May write protocols
May require travel to field sites
Possession of a Bachelor's degree from an accredited college/university according to the Council for Higher Education Accreditation (CHEA)
No experience required with Bachelor’s degree
Ability to lift and carry up to 25lbs
ELISA
Excellent verbal and written communication/customer service skills

112

Clinical Research Associate Resume Examples & Samples

Designs, plans and implements the overall direction of clinical research projects
May draft materials including informed consent documents, draft source documents, patient instruction guides and case report forms (CRFs)
Assists with the recruitment of research participants and the collection, management, and analysis of specimens and data
Assists with protocol development and contributes to the preparation of regulatory submissions to the Institutional Review Board (IRB)
Monitors intramural research protocols and ensures the clinical trials are conducted in accordance with Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), and all applicable regulatory guidelines
Assists with opening, monitoring, and closing studies, clinical site management, and managing the relationship with Clinical Research Organizations (CROs) and field CRAs
Ensures appropriate reporting of Adverse Events (AEs) and Serious Adverse Events (SAEs)
Reviews clinical trial data for quality and completeness
Tracks patient enrollment, randomization, and drug dispensing
Ensures the safety and confidentiality of study subjects
Interacts with internal and external staff to facilitate project timelines
Assists in preparing documents to be submitted to the Food and Drug Administration (FDA), as well as annual protocol reports, manuscripts, and abstracts for publication
Attends laboratory and clinic meetings, clinic conferences, and other seminars/meetings
Travels occasionally for domestic and international conferences
Acts as the liaison to NIH and CNMC staff to ensure clinical trials are well coordinated
Coordinates and guides patients through study visits and is the Point of Contact (POC) for patients associated with the different studies
Works in collaboration with the Study Coordinators and Case Managers associated with the studies
Possession of a Bachelor’s degree from an accredited college or university according to the Council Higher Education Accreditation (CHEA) in a field related to biomedical research, clinical trials and/or health, or four (4) years related experience in lieu of degree
Must be able to obtain and maintain a Public Trust Clearance
Biomedical research or clinical related experience may be substituted for the degree
Ability to work in a clinical research setting both independently and within a team environment
Must be detail-oriented and possess strong organizational skills with the ability to prioritize multiple tasks and projects
Ability to communicate effectively, orally and in writing, with non-technical and technical staff
Familiarity with FDA regulatory requirements and guidelines for clinical research, as well as monitoring requirements
Infectious disease experience
Knowledge of Department of Health and Human Services regulations
Experience with the development of CRFs, FrameMaker® and TrackWise®

113

Senior Clinical Research Associate Resume Examples & Samples

Will assist the Clinical Project Manager and/or Clinical Affairs representative as a team leader on assigned project teams to provide clinical guidance, strategy, and support for the development of new technologies, new products, and extended product claims
Assist in the design and develop key clinical study documents (e.g. informed consent forms, monitoring plans) ensuring that the study will produce sound and thorough data to support the approval process; seek input as needed from cross-functional team members
Oversee and adhere to study protocol, budget and timeline
Ensure maintenance of clinical project files to ensure compliance with internal procedures, and applicable country-specific regulations
Serve as a clinical expert to study site staff, investigators, sales representatives, and other staff members regarding investigational products and protocol
Involved in the preparation of documents for publications, submissions and the coordination of submissions
Effectively identify, build, and leverage effective relationships with external advisors, clinical investigators, vendors, and applicable research staff
Provide project updates to effectively communicate to management on a regular basis
Participate in work streams and or process improvement initiatives
Develop training materials and serve as mentor to CRA staff
Strong understanding of cardiovascular anatomy, pathology and physiology
Able to coordinate and lead multiple projects simultaneously in a fast-paced work environment

114

Clinical Research Associate Resume Examples & Samples

Assess adequacy of potential clinical investigators and clinical trial sites.Includes evaluation of facilities, personnel, patient referral base, and adherence to GCP/ ICH
Act as one of the primary contacts between Seattle Genetics, Contract Research Organizations (CROs), vendors, and multiple clinical trial sites.Maintain close contact with clinical trial sites
Must be willing to travel (< 10 – 20%)

115

Senior Clinical Research Associate Resume Examples & Samples

Experience in Immunology monitoring is preferred
Proven strong site management and monitoring skills
Good negotiating skills, tact and diplomacy

116

Senior Clinical Research Associate Resume Examples & Samples

Job Description
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
 Strong knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
 Strong therapeutic and protocol knowledge as provided in company training
 Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer
 Strong written and verbal communication skills including good command of English language
 Strong organizational and problem-solving skills
 Effective time management skills
 Ability to manage competing priorities
 Good mentoring and training skills
 Ability to establish and maintain effective working relationships with coworkers, managers and clients
Page 2
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
 Bachelor's degree in a health care or other scientific discipline or educational equivalent and 2 years of on-site monitoring experience; or equivalent combination of education, training and experience”

117

Senior Clinical Research Associate Resume Examples & Samples

Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
Act as a mentor for clinical staff including conducting co-monitoring and training visits
May provide assistance with design of study tools, documents and processes
Strong knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Strong therapeutic and protocol knowledge as provided in company training
Strong organizational and problem-solving skills
Good mentoring and training skills
Bachelor's degree in a health care or other scientific discipline or educational equivalent and 2 years of on-site monitoring experience; or equivalent combination of education, training and experience”

118

Clinical Research Associate Resume Examples & Samples

Participates in the investigator recruitment process. Performs site evaluation visits of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study
Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Works with sites to resolve data queries
Perform SAE review and reconciliation
May review protocols, eCRFs, study manuals and other related documents, as requested by Clinical Trial Manager and/or Lead CRA
Serves as primary contact between Novella and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested
Authorized to request site audits due to data integrity concerns
Ensure internal and study-related training's are completed per Novella and/or study timelines; CTMS should be current at all times with the pertinent site updates/contacts
Participate in the investigator recruitment process. Perform site evaluation visits, as needed, of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study
Assist CTM and/or PM in review of project budgets, monitoring costs, potential overruns and propose/implement cost effective solutions
Review and approve CRA travel expenses and time sheets
Must possess 2+ years of oncology and/or medical device experience

119

Clinical Research Associate Resume Examples & Samples

Working as part of an international clinical team which is led by the Clinical Trial Manager
To ensure appropriate attention is provided to the sites in order to drive data quality so that the clinical study protocol requirements are fulfilled within the appropriate regulatory and ethical framework
Knowledge of local regulatory, ethics and institutional contract procedures and submissions
Demonstrated experience of performing site start up procedures, routine monitoring and site closure
Excellent interpersonal and organisational skills
Ability to manage multiple priorities across various clinical trials
Fluency in both French and English (spoken and written) is essential
Valid drivers’ licence and ability to travel throughout France and Belgium

120

Lead Clinical Research Associate Resume Examples & Samples

Understanding of current GCP/ICH guidelines applicable to the conduct of clinical research
BS/BA (or equivalent) in one of the life sciences with a minimum of 4 years of monitoring experience or equivalent amount of education/experience
Must possess excellent verbal and written communication, interpersonal and organizational skills
Requires an ability to work independently, prioritize, and work within a matrix team environment

121

Senior Clinical Research Associate Resume Examples & Samples

Collaborates with the ISSC department to coordinate activities with the site in preparation for the initiation of the study. Obtains regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Works with ISSC and site staff to obtain regulatory (IRB/IEC) approval of study specific documents
Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF; monitoring activities and study close-out activities
Collaborate with the ISSC department to coordinate activities with the site in preparation for the initiation of the study. Obtains regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Works with ISSC and site staff to obtain regulatory (IRB/IEC) approval of study specific documents
Perform study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF; monitoring activities and study close-out activities
Assist the study management in identifying and generating changes in scope
Serve as mentor for junior CRAs and those new to the company and/or study
Excellent, presentation, organizational and interpersonal skills
For the Technical CTM role, the CRA must have a deep understanding of Novella systems with the ability to learn even more

122

Senior Clinical Research Associate Resume Examples & Samples

In the country/region based, manages activities of clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol
Conducts all clinical site activities according to the monitoring plan and in accordance with the study timelines and company objectives
Identifies and communicates issues that impact resource allocation and provides solutions
Anticipates and identifies site issues that could affect timelines and develops alternative solutions
Provides input to forecast resource requirements for assigned clinical studies in the country(ies) responsible for
Works in partnership with study teams to resolve critical and complex issues with study conduct at clinical sites
Under direction of the Clinical Operations Manager and/or Senior Clinical Operations Manager, provides strategic direction, advice and guidance to assigned local Site Management & Monitoring staff in relation to clinical operations responsibilities and activities; promotes best practice; enables provision of quality local services to AbbVie; identifies infrastructural improvements and implements action plan to ensure Site Management & Monitoring and business objectives are successfully met; ensures alignment of local Site Management & Monitoring activates with regional/global initiatives
Ensures project implementation within country(ies)/region(s)/responsible for
Provides hands-on assistance to assigned staff for project implementation as needed
May participate in global Task Forces and Initiatives
Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs_ and to quality standards in conducting clinical research are maintained
Ensures that compliance requirements to competent authorities and HQ are met
Participates in the development of local SOPs or working instructions as needed, interacting with appropriate local functions
Work with appropriate staff to ensure that clinical trial management systems containing all study-specific information are maintained and kept current
Track and manage performance metrics for assigned monitoring staff
Ensures financial information for assigned studies/sites is entered into company systems in a timely manner and is managed in compliance with company policies (ex-US)
Candidate should be located in Maryland

123

Clinical Research Associate Resume Examples & Samples

Ensures regulatory inspection readiness at assigned clinical sites
Conducts all clinical site monitoring activities according to the monitoring plan and in accordance with the study timelines and company objectives. This includes but is not limited to
Overviews the overall activities of site personnel over whom there is no direct authority and motivate/influence them to meet study objectives. Is proactive in managing the site and ensures action plans are put into place as needed to ensure compliance
Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations
Prepare and submit written reports, both monitoring and administrative, in a timely, concise and objective manner
Employs good financial management to conserve costs of departmental operation and control travel expenses, with guidance from Senior ACOM/COM/Sr COM as appropriate
Manages investigator payments as per executed contract obligations. Negotiates investigator/ hospital agreements with stakeholders
Maintain and complete own expense reports as per local and applicable guidelines
Identifies, evaluates and recommends new/potential investigators/sites on an on going basis
Creates a positive work environment by encouraging mutual respect, innovation, and accountability at all levels
Candidate should be located in New York
Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing) preferred
Minimum of 1 year of clinically-related experience, of which a period of 6 months is preferable in clinical research monitoring
Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials
Experience in on-site monitoring of investigational drug or device trials is required
Competence in the use of personal computers, including experience with word processing, spread sheets, email and web-browser applications

124

Clinical Research Associate Resume Examples & Samples

Research experience in investigational drug trials preferred
Skilled in organization and implementing requirements of research protocols
Knowledge of the design, conduct and critical review of clinical trials with the appropriate skills required performing the functions of the positions
Phlebotomy license/skills required

125

Senior Clinical Research Associate Resume Examples & Samples

Maintains required and functional job specific training
Performs other work-related duties as assigned
Acts a representative of the Company, demonstrates professional attire, attitude and behavior in meetings & teleconferences, site visits and interactions, and interpersonal activities in general
BA/BS degree in science/health care field or nursing degree or equivalent combined education and experienceBA/BS degree in science/health care field or nursing degree or equivalent combined education and experience
Extensive experience as a CRA with a thorough understanding of SOPs, WIs, FDA and local regulations as well as ICH-GCP guidelines
On site experience: signed off on all types of visits; PSSV, SIV, IMV, COV. Experience of Observation/Training visit on all types of visits
Experienced at independent drug accountability and evidence of proactive identification / escalation / resolution of any issues found
Experienced at independent investigator site file review and evidence of proactive identification / escalation / resolution of any issues found
Off-site experience: mastery of basic category and familiarity with complex category of Clinical Monitoring Associate tasks
Comfortable in navigation within, and able to assist junior staff in: CTMS systems, Data Platforms for assigned projects, Microsoft Suite: Excel, Word, Power Point, Outlook, Site EMR systems
Model consistent professional maturity as represented by: Approaching mastery of professional communication in interpersonal and written work
Demonstrating conflict management skills such that the CRA is able to navigate challenging site relationships successfully
Ability to cultivate strong relationships and establish credibility to influence others in situations without direct authority
Has good knowledge of Strategic Data Monitoring

126

Clinical Research Associate Resume Examples & Samples

The main purpose of this role will be to perform all required activities to ensure appropriate monitoring of investigator sites and study execution under the supervision the Manager Clinical Field Operation
The Senior Clinical Research Associate (SCRA) implements and coordinates assigned clinical research projects in EMEAC
The SCRA ensures that activities are conducted in accordance with the internal quality system and external guidelines and regulations. SCRA ensures that the projects are conducted according to protocol and associated documents and that agreed study milestones and timelines will be achieved. The SCRA needs to adhere to Monitoring Plan
High education degree in a scientific, health care, or other related discipline required
Minimum of 2 years of monitoring experience in the cardiovascular field
Submission experience to the regulatory bodies and Ethical committees in Spain
Excellent knowledge of written and spoken English, Spanish and French
Flexibility to travel (up to 70% of the time)

127

Senior Clinical Research Associate Resume Examples & Samples

Perform all required activities to ensure appropriate monitoring of investigator sites and study execution under the supervision the Manager Clinical Field Operation
The SCRA is responsible for the management of day-to-day aspects of study sites for the assigned projects and provides updates to the study team
Minimum of 4 – 5 years field monitoring experience

128

Clinical Research Associate Resume Examples & Samples

Conducts Site Qualification, Initiation, Interim Monitoring, Close-Out visits and activities in accordance with FDA Code of Federal Regulations, Good Clinical Practice, guidelines, departmental procedures and the Clinical Monitoring Plan (CMP)
Prepares and completes monitoring visit reports and letters, and effectively document site communications Identify and address routine site issues including protocol deviations, subject recruitment and retention programs and communicate any observed study /data trends and proposed resolution
Assists with the development of clinical trial documents
Provides leadership, training, and mentoring, as needed
Works on multiple projects and may function as a Study Lead
College Degree and minimum of 5-8 years of clinical monitoring experience

129

Clinical Research Associate Resume Examples & Samples

Coordinate the tracking of Essential Documents and key operational metrics for assigned studies
Perform Quality Control (QC) reviews of study documents to ensure that they are complete, accurate, and verifiable, and ensure that documents do not contain any PHI (Protected Health Information) in compliance with HIPAA requirements
Load and maintain study documents in Bard’s eTMF (electronic Trial Master File)
Interact with Investigational Sites to obtain study documents and related information
Update and maintain Bard’s Clinical Trial Management System (CTMS) for assigned studies to ensure accurate tracking of study contacts, vendor contacts and expiring study documents
Coordinate and participate in periodic review/audit of Trial Master Files to ensure that essential study documents remain complete, accurate, and verifiable
Assist in the development of study materials and tools to assist investigative sites during the clinical trial. Examples include regulatory and source document binders, template forms for Screen/Enrollment logs, Delegation logs, Device Accountability logs and training materials
Update and maintain project related systems, databases, tracking tools, timelines, and project plans (e.g., clinicaltrials.gov; SharePoint, etc.)
Under the direction of the study manager, coordinate investigational device inventory and accountability. This may include ordering devices from vendors for shipment to investigative sites, ensuring receipt at the site and tracking and accounting for all study devices at the end of the study
Coordinate the reporting and follow-up of reportable adverse events to Bard’s field assurance team
Prepare and distribute letters, memos, meeting minutes, and clinical administrative documents
Coordinate the receipt and processing of invoices, purchase orders, and purchasing requisitions, and track site/vendor payments
Coordinate project team meetings as needed (e.g., schedule rooms, coordinate logistics, prepare agendas, prepare/distribute minutes, etc.)
Strong organizational skills and a keen attention to detail
The ability to interpret and analyze a broad range of technical documentation
The ability to work independently at times with minimal supervision
Strong oral and written communication skills with an ability to proofread technical documentation for correct grammar, syntax, and spelling
Proven ability to prioritize multiple tasks in a fast-paced business environment
Proven ability to plan work and complete assignments on time
The ability to maintain confidentiality about information received in the course of duties
Strong computer skills with experience in Microsoft Outlook, Word, Excel, Access, Project and PowerPoint, and the ability to quickly learn and navigate Bard’s internal network systems (e.g., CTMS, SharePoint, etc.)
Knowledge of GCP-ICH and International regulatory requirements governing medical device research and development
Prior experience coordinating industry sponsored clinical studies

130

Clinical Research Associate Resume Examples & Samples

85% - Clinical Trial Support (May include but not limited to activities listed)
Assist in providing oversight of CRO activities regarding country and site specific informed consent documentation tracking, finalization and approval
10% Departmental Tasks
1-3 year's experience in similar/relevant field (eg.Sponsor, CRO, Clincal trial Vendor, Clincal Coordinator, etc.)

131

Senior Clinical Research Associate Resume Examples & Samples

Assume ambassadorial role to facilitate communication between sites and Novartis line functions and increase value proposition to investigators
Facilitate preparation and collection of site level documents; resolve problems as required
Execute site initiation and training
Implement total site management including monitoring visits, regulatory assessment, drug supply management and resolution of site problems to ensure compliance
Track trial execution milestones; identify problems; resolve issues and escalate as appropriate
Manage recruitment and execute contingency plans, as needed. 8. Complete preparation/generation of study monitoring reports
Manage data at the site; resolve technical and content issues to achieve aggressive database lock targets
Implement site closeout activities
Act as local and/or global CRA lead and author global monitoring plan
Act as a mentor to new associates for purposes of field training, as assigned
Participate in multi-disciplinary teams within CPO and globally to evaluate and implement process improvements
Foster sound working relationships with both internal and external customers

132

Clinical Research Associate Resume Examples & Samples

Participate in initial and on-going protocol and CRF training
May serve as the primary contact for the clinical sites/sponsor
Participate in the generation of study specific monitoring plans
May assist in the development of protocols and Case Report Forms
Participate in sponsor and investigator/initiation meetings
Tracks progress of assigned studies projects and identifies appropriate actions to achieve target objectives
Fulfill on-site monitoring responsibilities
Ensure that study staff conducting the protocol have received the proper materials, instructions and training to safely enter subjects into the study and complete the protocol requirements, as written
Ensure the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
Ensure the integrity of the data submitted on CRFs or other data collection tools by careful source document review
Ensure that the site regulatory documents are complete and current throughout the duration of the trial
Ensure that the study investigational product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements
Identifies and completes follow up of SAEs at study site for which he/she is responsible
Independently performs CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems
Typically 2 years of experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, or data management)

133

Clinical Research Associate Resume Examples & Samples

Minimum of two (2) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)
Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
Fluent in local office language and in English, both written and verbal

134

Clinical Research Associate Resume Examples & Samples

Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
Excellent registry administration skills
Good planning and organization skills
Good computer skills with good working knowledge of a range of computer packages

135

Clinical Research Associate Resume Examples & Samples

Responsible for study startup which include IRB/IEC submission, site selection, recruitment of potential investigators, notifications to regulatory authorities, translation of study-related documentation
Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned
Responsible for all aspects of site management as prescribed in the project plans
Complete Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
Independently perform Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by management
May support in organization of meetings and other tasks as instructed by supervisor
Minimum of two (2) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits) with 1 year of phase I monitoring experience is preferred
Good communication, interpersonal, analytical and negotiation skills

136

Senior Clinical Research Associate Resume Examples & Samples

In lieu of the above requirements, candidates with > four (4) years supervisory experience in a health care setting and three (3) years clinical research experience in the pharmaceutical or CRO industries (including monitoring) may be considered
Excellent site monitoring skills
Excellent study site management skills
Ability to train and supervise junior staff
Ability to resolve project-related problems and prioritizes workload for self and team

137

Senior Clinical Research Associate Resume Examples & Samples

Recruiting potential investigators, preparing EC submissions, translating study-related documentation, organizing of meetings and other tasks as instructed by supervisor
Interact with internal work groups to evaluate needs, resources and timelines
Assist with training, mentoring, and development of junior employees, e.g. co-monitoring
Serve as lead monitor for a protocol or project and may assist in establishing monitoring plans as assigned
Minimum 4 years of relevant clinical research experience in pharmaceutical or CRO industries
Experience in different therapeutic areas with the emphasis on oncology (3 years)

138

Senior Clinical Research Associate Resume Examples & Samples

Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
Minimum of Four (4) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)
Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs

139

Senior Clinical Research Associate Resume Examples & Samples

Assisting with training, mentoring, and development of new employees, e.g. co-monitoring
Previous clinical research experience in pharmaceutical or CRO industries
Fluency in Hungarian
Very good knowledge English language

140

Clinical Research Associate Resume Examples & Samples

Minimum 2 years of monitoring experience (including pre-study, initiation, routine monitoring and closeout visits) - oncology experience highly preferred
Oncology experience is a definite plus
Fluent in English and local language, both written and verbal

141

Clinical Research Associate Resume Examples & Samples

Monitoring skill, site management skill, communication skills
Good planning and organization skill, computer skills
Ability to resolve project related problems and priorities workload and work in a team

142

Clinical Research Associate Resume Examples & Samples

Meets all requirements of the Clinical Research Associate (I) level
Assists with the implementation of Project Plans related to the Clinical Monitoring responsibilities
Participates in initial and on-going protocol and CRF training at study site
May serve as the Primary contact for the clinical sites/Sponsor
Participates in the generation of study specific monitoring plans
May participate in the development of Case Report Forms
Participates in the development of and/or review of conventions for CRF transcription
May develop materials for site reference manual
May participate in identification and recruitment of investigators, collection of investigator documents and Pre-Study Visits
Participates in Sponsor and Investigator/Initiation Meetings
Tracks progress of assigned studies/projects and identifies appropriate actions to achieve target objectives
Fulfills general on-site Monitoring Responsibilities
Typically 2 - 4 years of experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, or data management)
Typically 1 - 2 years Clinical Monitoring experience
Additional experience may be substituted for monitoring experience – specifically, experience in the role of Research Nurse or Clinical Research Coordinator can be substituted for experience in Clinical Monitoring, provided the incumbent participants in a comprehensive program of monitoring skills training provided by Covance at the outset of employment, and demonstrates proficiency in monitoring skills via assessment prior to independent conduct of clinical monitoring activities
Proficient computer skills with good working knowledge of a range of standard computer software required (e.g. email, document, spreadsheet and presentation software)

143

Senior Clinical Research Associate Resume Examples & Samples

All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits
Degree educated (Life Science)
Few years of relevant clinical research experience in pharmaceutical or CRO industries
Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries
Full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
Fluent Norwegian and English language skills

144

Clinical Research Associate Resume Examples & Samples

Ideally minimum of 2 years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits) at a CRO or Pharmaceutical environment
Fluency in German and English. Able to monitor in either French or Italian
Strong background in IT applications and E-CRF experience
Training skills to train sites to perform excellent
A valid driving license
Available for travel up to 60% of the time, including overnight stays as necessary

145

Senior Clinical Research Associate Resume Examples & Samples

The clinical research associate will be responsible for ensuring that the sites used for clinical studies meet ICH GCP requirements
CRAs will visit clinical trial sites for pre-qualification, site initiation, interim monitoring and site closeout
The CRAs are also responsible for documenting study visits, and participate in study planning and coordination
Bachelor's Degree required, certification as a CRA or clinical research professional highly desired
Experience monitoring sites for human clinical trials, site initiation, monitoring, and closeouts desired
Attention to detail is critical as well as excellent oral and written communication.Search Jobs US

146

Clinical Research Associate Resume Examples & Samples

Undertake feasibility work when requested
Minimum 2 years of relevant clinical research experience in pharmaceutical or CRO industries
Knowledge of Hungarian, Romanian and English languages is a must
Contract negotiation experience
Understanding of the clinical trial process

147

Clinical Research Associate Resume Examples & Samples

Ensures adequate documentation and proper implementation of written protocols
Serves as a liaison between Align Technology and the study site, investigators, study coordinators, staff members
Provides technical assistance to study sites regarding the conduct of clinical research
Oversees delivery and shipment of aligners for clinical studies
Follows all departmental and company procedures as indicated in quality, administrative, or other systems
Comply with all safety policies, practices and procedures. Report all unsafe activities to supervisor and/or Human Resources
Travel may be required – up to 15%
1-2 year experience as a Clinical Research Associate
Ability to think critically and scientifically
Ability to write clinical reports and protocols

148

Senior Clinical Research Associate Resume Examples & Samples

Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors, responsible for all aspects of site management and registry management as prescribed in the project plans
Organize and make presentations at Investigator Meetings
Preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned

149

Senior Clinical Research Associate Resume Examples & Samples

May assist with, and attend, Investigator Meetings for assigned studies
May serve as mentor for new clinical study monitors
Attend study-related, company, departmental, and external meetings, as required
Conduct Field Evaluation Visits and field training of CRA Is, IIs and Sr CRAs
Working knowledge of all functional areas of clinical trials and medical terminology

150

Senior Clinical Research Associate Resume Examples & Samples

Take charge of all aspects of Site Management as prescribed in the project plans
Negotiate study budgets with potential investigators and collaborate with the Covance legal department with statements of agreements as assigned
Ability to monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP and ICH Guidelines
Senior CRA positions require 4+ years of clinical research monitoring experience. Alternatively candidates with 4+ years supervisory experience in a health care setting and 3+ years clinical research experience in the pharmaceutical or CRO industries (including monitoring) may also be considered
Minimum of three (3) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)
In lieu of the above requirements, candidates with > three (3) years supervisory experience in a health care setting and two (2) years clinical research experience in the pharmaceutical or CRO industries (including monitoring) may be considered
Ability to resolve project-related problems and prioritizes workload for self

151

Lead Clinical Research Associate Resume Examples & Samples

Conducts trip report review for assigned projects
Tracks visit and trip report metrics and summarizes/reports to teams; creates and implements tracking tools, as needed
Tracks utilization of visits against the budget in conjunction with the study Project Manager/Clinical Trial Manager
Manages monitoring needs of the study and initiates proposed solutions to CRA managers if additional CRA resources are needed
Reviews site data quality trends via trip reports and data review including queries and protocol deviations
Assists the Project Manager/Clinical Trial Manager with UAT testing and eCRF guideline review
Reviews site feasibility questionnaires in preparation for Pre-Study Visits (PSVs) and site selection
Participates in CRA project-specific training
Supports face-to-face sponsor meeting preparation and may develop materials related to the training and presentations for Investigator Meetings; may present at meetings
Develops Clinical Monitoring Plans with review from the CRA Manager
Develops Monitoring tools, Source Document Templates, and trip report annotations with review from the CRA Manager
Facilitates CRA project meetings (agenda and minutes) and is the primary responsible for communicating study information to the CRAs; may work with the Project Manager/Clincial Trial Manager to facilitate these meetings
Provides a key role in problem solving and issue escalation, regarding monitoring issues, with proposed solutions to Project Management team and Sponsor as needed
Mentors and co-monitors with CRAs on assigned team as needed
May observe the first SIV and conduct observation visits and co-monitoring visits to address site and CRA performance needs
Conducts all types of clinical monitoring visits (i.e., pre-study, initiation, interim and close-out) which includes all preparatory and follow-up aspects
Attends weekly sponsor/project management teleconferences
Involved in initial review of study documents, eg, protocol, CRFs, source documents, drug accountability, and informed consent
Monitors site performance and compliance and provide management with necessary reports, updates and recommendations
Assists sites and data management with data query resolution
Travels as required by study and site/CRA performance
Miscellaneous duties, as necessary, in support of Clinical Monitoring initiatives and business priorities and objectives
Excellent written and verbal communication skills in order to effectively communicate to a wide variety of audiences including senior management
Ability to anticipate study monitoring needs and provide solutions to the CRA Manager and project team
Ability to travel as needed (10-20%)

152

Clinical Research Associate Resume Examples & Samples

W2 Employees Only - Must have Device experience**
At least 5 years related experience in (conducting) clinical trials (healthcare setting , CRO, medical device and/or pharmaceutical company and/or industry)
Experience in electronic data capture and clinical trial management systems

153

Clinical Research Associate Resume Examples & Samples

Conducts all types of clinical monitoring visits (i.e., pre-study, initiation, interim and close-out) which include all preparatory and follow-up aspects, with oversight, as needed)
Attends weekly project CRA teleconferences, as appropriate
Monitors site performance and compliance and provides LCRA with necessary reports, updates and recommendations
Prepares clinical sites for regulatory agency audits
Travels as required by study
Develops subject recruitment strategies and works with sites on meeting enrollment timelines
Performs miscellaneous duties, as necessary, in support of Clinical Monitoring initiatives and business priorities and objectives
Detailed knowledge of FDA regulations and GCP/ICH guidelines as they apply to the conduct of clinical research
Ability to travel on a regular basis
Working knowledge of Microsoft Office Suite

154

Senior Clinical Research Associate Resume Examples & Samples

Able to complete complicated tasks high independently, able to perform and lead study specific
Bachelors degree in clinical medicine or a life/biological science
Good computer skills including proficiency with Microsoft Word, Explorer and Outlook and

155

Senior Clinical Research Associate Resume Examples & Samples

Assist with management of third party vendors
Monitor and manage study sites, as necessary
Track and prepare study- specific information utilizing databases, spreadsheet and other tools
Assist in the development, assembly and distribution of study documents, manuals and tools
Reporting of study issues to Sr. Manager or Clinical Operations Director/Sr. Director
Maintains and manages internal clinical trial files and documents
Coordinates and plans for the availability of non-clinical supplies necessary to meet study requirements
Travel to sites when necessary (~50%)
The candidate must have a BA/BS degree or equivalent; health science degree or biologic science degree is preferred. A minimum of 5 years experience in the pharmaceutical industry, with minimum 3 years direct experience in monitoring and managing study sites
The candidate should have significant experience with responsible roles in the conduct or management of Phase I – III clinical trials
The candidate should be detail-oriented, a self- starter and be comfortable with broad responsibilities in an

156

Senior Clinical Research Associate Resume Examples & Samples

Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visit; liaise with vendors; and other duties, as assigned
Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
Ensure the protection of study patients verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
Ensure the integrity of data submitted on Case report Form (CRFs) or other data collection tools by careful source document review. Monitor data for missing or implausible data
Manage small projects under direction of a Project Manager/Director as assigned
Serve as lead monitor for a protocol or project and may assist in establishing monitoring plan as assigned
External Candidated
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure),

157

Clinical Research Associate Resume Examples & Samples

Management of Australasian clinical investigator sites from site identification through start-up, recruitment & maintenance and close-out as part of local or global clinical studies according to ICH GCP guidelines and GSK SOPs
Clinical Trial Document management
Involvement in negotiating financial arrangements with sites within agreed limits, document financial agreements accordingly and co-ordinate timely payments to sites
Setup, co-ordinate and contribute to investigator meetings when necessary
Maintain good communication and working relationships with investigators, other site staff, overseas colleagues, external customers and other GSK staff
Uphold and promote the company externally by demonstrating high professional standards and integrity in all external contacts
Involvement in the regular review of procedures and practices involved in planning, set-up, monitoring and co-ordinating clinical trials
Make recommendations for improvements to your Manager
Be familiar with relevant therapeutic areas and clinical research procedures by attending both core and on-going training sessions, reading/viewing relevant materials and by discussion with internal and external experts
Tertiary qualification in health, social and/or biological science, pharmacy
Some prior Clinical Research Associate experience
Well developed verbal and written communication skills
Excellent interpersonal skills; including the ability to competently liaise with and feedback to internal and external customers regarding project issues and company decisions
Attention to detail and ability to work to achieve required timelines
Commitment to continuous learning and improvement
Ability to negotiate with and motivate others

158

Senior Clinical Research Associate Resume Examples & Samples

Conducting on-site Accompanied Field Visit activities (Quality Control Visits) for CoSource staff
Effectively communicating management strategies, policies and procedures in conjunction with leadership teams
Developing and maintaining effective relationships with client management teams to manage CoSource staff in a matrix environment
Maintaining good working relationships with internal and external clients to ensure opportunity for supporting additional new business
Forecasts country resource needs
Oversees country and site validations, site selection and recruitment in assigned protocols responsible for clinical trial education to sites
University/college degree (life science preferred), or certification in a related allied health profession
In lieu of the above requirement, candidates with several years of relevant clinical research experience in pharmaceutical or CRO industries will be considered
Fluent in local office language and in English
Relevant clinical research experience in a pharmaceutical company or CRO
At least 4 years of monitoring experience
Ability to effectively conduct clinical studies and develop the pipeline
Maintaining local regulatory and compliance requirements in countries
Ability to make decisions independently and oversee important activities relevant to clinical research activities in the country according to predetermined global policies and commitments with the support
Strong understanding of local regulatory environment
Ability to identify problems, conflicts and opportunities early and lead
Communication and empathic skills
Ability to coordinate and lead local teams to high performance

159

Clinical Research Associate Resume Examples & Samples

Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters in a timely manner using approved Novella/sponsor forms and reports
Authorized to request site audits for reasons of validity
Understanding of basic data processing functions, including electronic data capture

160

Clinical Research Associate Resume Examples & Samples

CM_Data_Cleaning_Report_By_Site and CM_Data_Cleaning_Report_By_Subject both Business Objects reports
Reconcile patients that have come off treatment and off study
Generate and review various IL2 reports
Works closely with CDRC to ensure data is further reviewed and discrepancies documented
The Technical CTM may participate in CDRC review and aid in Patient Profile review, as necessary
There may be additional tracking required as a result of CDRC’s review

161

Senior Clinical Research Associate Resume Examples & Samples

Support all clinical research activities essential to the successful management of pre and post –market clinical studies under the direct supervision of clinical project manager or clinical affairs director
Maintain and track data of the clinical studies including investigator selection, analysis of potential patient recruitment, and overall study status/progress throughout the life of a study
Manage site start-up/activation process, including: preparation of study related documents (protocols, case report forms/eCRFs, Informed consents, Clinical trial agreements), organizing IRB/EC submissions and applicable regulatory documentation with follow through to ensure successful outcomes
Amends clinical study documents as needed
Monitor (remotely) clinical study data entered in an Electronic Data Capture (EDC) system or paper case report form at sites to ensure regulatory and protocol compliance as well as overall accuracy
Serve as main liaison to participating clinical trial sites with focus on data entry, query resolution and overall site activity
Conduct clinical study site monitoring, as required
Provide project administrative support including maintenance of study documentation (e.g., correspondence, CRFs, study approval documents), trip reports, site contact documentation, monthly status reports (e.g., enrollment, adverse events, budget, etc.) and, as required, prepare clinical summaries
Oversee purchase order process and invoice reconciliation for clinical studies as well as the Clinical Affairs department, including working with accounts payable and external parties
Assist Clinical Project Managers with development of Clinical Evaluation Reports (CER), including evaluating and summarizing Medical Device Vigilance Reports (MDVRs) and assisting with clinical literature search and appraisal
Partner with Clinical Project Managers on study scoping activities, including but not limited to development of pre-study questionnaires, study design and surgeon/site selection
Lead clinical quality initiatives including internal compliance audits of current clinical studies, and review of quality system documents including DOPs, SOPs and Work Instructions
Possess basic knowledge of Good Clinical Practice and 21 CFR Part 11 and international regulations
Bachelor’s degree in scientific field required
Clinical research/clinical trial management certification/education preferred
Must be Clinically savvy
Experience in clinical trial management preferred (2-4 years)
Must be able to travel up to 10-20%
Good communication and interpersonal skills with high attention to detail and organization
Basic medical writing skills preferred
Proficiency in Microsoft Office, including Word, PowerPoint, Visio and Excel
Experience working with electronic data capture systems
Experience in medical device industry required

162

Senior Clinical Research Associate Resume Examples & Samples

Conducts periodic site file audits to ensure compliance with GCPs and Novella standard operating procedures
Assists with, attends, and may present at Investigator Meetings for assigned studies
Performs study close-out visits
At least four years experience in monitoring clinical trials preferred
Excellent organizational and interpersonal skills
Able to mentor other CRAs on project team and co-monitor as required
Computer literacy and knowledge of electronic data capture preferred
Must be able to travel domestically and internationally 50-75%

163

Senior Clinical Research Associate Resume Examples & Samples

Monitoring of moderately complex clinical experimentation including data collection, summary and thorough analysis, in support of department research projects and guidelines. Compose robust experimentation strategies that maximize effective use of resources and time to deliver optimum information
Apply knowledge of FDA regulations to site monitoring and clinical study design duties
Apply knowledge of Alere products to effectively train clinical sites before study initiation
Generate oral and written reports as necessary and to summarize clinical investigations and projects. Initiate communication with related staff and functions as necessary to coordinate activities effectively
Provide recommendations and observations to senior scientific staff on results of projects/tasks. Play a major role in the formulation of research strategies and tactics
Interact with study coordinators at clinical sites to ensure optimal study progression and resolve problems. Pro-actively recommend strategies to overcome hurdles
May functionally direct junior staff as required
Initiate literature review and searches to support ongoing research activities. Summarize findings in a final form to senior staff and recommend follow-up actions
Demonstrates commitment to the development, implementation and effectiveness of Alere Quality Management System per ISO, FDA, and other regulatory agencies
Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices
Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities

164

Clinical Research Associate Resume Examples & Samples

Position Title: Clinical Research Associate
Ensures site study supplies (such as Non-IP, lab kits, etc.) are adequate for trial conduct
Ensures that clinical drug supplies are appropriately used, handled and stored and returns are accurately inventoried and documented
Ensures site staff complete the data entry and resolve queries within expected timelines
Ensures accuracy, validity and completeness of data collected at trial sites
Maintains complete, accurate and timely data and essential documents in systems utilized for trial management (e.g. CTMS, eTMF/IF, Trial Master Source and Sharepoints
Fully documents trial related activities in particular monitoring. Writes visit reports and uploads into eTMF within 5 working days for review and approval. Complete follow-up letter to communicate relevant information and required corrective action to the investigator and his/her team with 15 working days. Promptly communicates relevant status information and issues to appropriate stakeholders
Collaborates with LTM for documenting and communicating site/study progress and issues to trial central team
Attends regularly scheduled team meetings and trainings
Works closely with LTM to ensure CAPA is completed for QA site audits and for quality issues identified at the site during routine monitoring and other visit types, e.g…,OSQMV
Prepares trial sites for close out, conduct final close out visit
Negotiates investigator budgets at site level, if applicable
Tracks costs at site level and ensure payments are made, if applicable
Leads and/or participates in special initiatives as assigned
May assume additional responsibilities or special initiatives such as “Champion” or Therapeutic Area Expert”

165

Lead Clinical Research Associate Resume Examples & Samples

Position Title: Lead Clinical Research Associate
Sector: Janssen
Collaborates with the CPL, GTM, local management/Country Head and Protocol Owner to select final site list
Contributes input to the development of Trial Plan, Safety Monitoring Plan, Filing and Archiving Plan and Investigational Product documents at a country level or initiates development of these plans for a single country trial
Leads and coordinates local trial team activities in compliance with GCO Standard Operating Procedures (SOP), Work Instructions (WI) and applicable regulations. Leads local project planning activities to meet recruitment targets and to deliver high quality data on time and within study budget. Including but not limited to: development of local trial specific procedures and tools, recruitment planning, contingency and risk management, and budget forecasting
Ensures that all SAEs/PQCs are reported within reporting timelines and documented as appropriate
Maintains and updates trial management systems - (e.g. CTMS, eTMF/LAF, Trial Master Source and Sharepoints).Uses study tools and management reports available to analyze trial progress
Monitors country progress and initiates corrective and preventive actions when the trial deviates from plans and communicates study progress and issues to study management teams
May submit requests for vendor services and may support vendor selection
May lead negotiation of trial site contracts and budgets. Forecasts and manages country/local trial budget to ensure accurate finance reporting and trial delivered –within budget. Adheres to finance reporting deliverables and timelines
Attends/participates in Investigator Meetings as needed. May schedule and conduct a local/country investigator meeting
Conducts local trial team meetings and provides or facilitates SM training when needed (i.e. implementation of study amendment-and changes in study related processes)
Reviews and approves Monitoring Visit Reports submitted by SM; identifies issues and/or trends across a trial project and escalates deviation issues to the GTM and FM as needed
Reviews and approves site and local vendor invoices as required
Works with SM to ensure CAPP is implemented for audits and inspection or any quality related visits
Complies with relevant training requirements
Act as local expert for assigned protocols. Develops strong therapeutic knowledge to support roles and responsibilities. May represent Global Clinical Operations on cross functional teams
Acts as primary local/country contact for a trial. Establishes and maintains excellent working relationships with external stakeholders, in particular investigators, study trial coordinators and other site staff; and internal stakeholders, including Medical Affairs and Marketing for Medical Affairs Trials
Actively contributes to process improvement; training and mentoring of Clinical Trial Administrators, Site Managers and other LTMs
May represent functional area in process initiatives
Contributes to optimization of daily processes

166

Clinical Research Associate Resume Examples & Samples

Regularly represents department in team meetings, leads teams and drive collaborative efforts (e.g., protocol development, CRO selection, etc.)
Oversees and is accountable for feasibility assessments for new studies
Responsible for TMF contents and accountable for TMF reconciliation
Oversees and is accountable for
2-4 years industry experience, including a minimum 4 years clinical research experience
Competent in the skills for the CRA II and the following

167

Clinical Research Associate Resume Examples & Samples

Maintain IRB documentation for clinical studies related to product development
Maintain clinical sub-study documentation
Coordinate and run in-house clinical studies, including recruitment of subjects, testing of subjects and completion of clinical report forms and IRB forms
Collaborate with the various project heads to design, plan and write protocols and SOP’s for in house studies
Conduct clinical studies ensuring compliance with the company’s SOP’s, IRB rules and standard clinical practice
Create and maintain and organize accurate study documents, logs, and binders
Prepare status reports, track progress and provide clinical feedback to project heads and team members
Maintain the viability of the physical set-up of the clinical lab, ensuring the safety and comfort of the subjects and all personnel who conduct and participate in study testing
Assists with site initiation, training and monitoring of external study sites and Beta sites as needed
Conduct clinical audits as necessary to support clinical studies, both internal and external
Participate as a member of Project Teams, as assigned

168

Clinical Research Associate Resume Examples & Samples

Prepare various clinical operation metrics and analytical reports; prepare abstracts/articles for investigators involved in ResMed's clinical studies; develop clinical study protocols and amendments
Develop and conduct presentations with designated groups, including investigators meetings, site personnel and internal ResMed teams
Development of study related documents according to study requirements, such as informed consent forms, case report forms, source documents, logs, newsletters, etc
Provide forecasting of clinical supplies with updated projections based on actual study information after study initiation
Conduct clinical study visits (site qualification, site initiation, interim monitoring and close out) in accordance with Good Clinical Practice (GCP), ResMed work instructions (WIs) and all state and federal regulations
Conduct potential site interviews and complete site selection process
Coordinate and participate in investigator meetings, site initiation and training of site staff
Collect and track regulatory documents (clinical trial research agreements, investigator's agreements, CVs, NDA, etc) for clinical studies per ResMed WIs
Assure clinical studies are conducted in accordance with the protocol, GCP, ResMed WIs and all applicable (e.g. FDA) regulations
Implement strategies for enrolment to ensure timely completion of clinical studies, in alignment with department and corporate strategic objectives (newsletters, conference calls, emails, etc)
Maintain up-to-date site and in-house regulatory documentation for the Trial Master File
Assist Medical Affairs management in the processing of adverse events, protocol deviations, and technical observations
Conduct data management activities (second review of CRFs, query processing, data analysis, etc)
Ensure adverse event, technical observations and protocol deviations are completed in accordance with ResMed WIs
Assist with posting and management of clinical studies on clinicaltrials.gov
Assist with the resolution of audit findings
Provide study summaries for Medical Affairs management, including reports, graphs and tables, as requested
Support budget and contract negotiations with clinical sites
Assist with selection of vendors and contractors, as needed
Assist with regulatory submissions, which include annual report, 510(k), PMA, and IDE submissions
Manage the operations of a clinical study, including newsletters, site conference calls, communication with investigators and study staff
Develop and manage tools/metrics for study progress (e.g., timelines, enrollment goals/graphs, etc)
Follow FDA and international regulations pertaining to medical devices and industry guidelines related to regulatory submissions, institutional review boards (IRB), clinical investigations, monitoring procedures and medical device reporting
Review clinical publications
Achieve high level of clinical expertise in various therapeutic areas and procedures associated with ResMed projects
Maintain knowledge base of clinical regulations for conducting trials
Develop and revise departmental procedures
Strong analytical, organizational, and communication skills
Outstanding time management and organization skills
Track record of successfully managing a team
Confident team leader and team builder with strong motivational skills
Adept in problem solving and resolving conflict
Able to manage internal customer relationships and expectations
Ability to travel 30-40% of the time
Must have excellent organizational skills and take ownership of work
Experience in communicating with all levels of management
Bachelor's Degree in Medical Science, Science or Life Science degree required; Masters degree in a relevant field preferred
Must have a minimum of 3 years of experience in clinical study support as a Clinical Research Associate (CRA) or Clinical Research Coordinator
Medical device study experience preferred and/or clinical experience in healthcare preferred
Knowledge about the practice of sleep and respiratory medicine a plus
Proficiency in Microsoft Office (Word, Excel, Power Point, Visio or equivalent flowcharting software, and Outlook) and Internet searches
Experience in relational database system such as Microsoft Access and publishing software such as Microsoft Publisher is desirable
Experience with electronic data capture systems is desirable

169

Senior Clinical Research Associate Resume Examples & Samples

Serves as a trainer for contract research organizations (CROs) needed for additional monitoring support
Ensures timely collection of study documentation by obtaining, maintaining and controlling all necessary records and documentation according to procedures and regulations
CORE LAB MANAGEMENT EXPERIENCE IS REQUIRED FOR THIS POSITION

170

Clinical Research Associate Resume Examples & Samples

Recruit potential investigators, prepare EC submissions, notify regulatory authorities, translate study-related documentation, and organize meetings and other tasks as instructed by supervisor
Independently perform CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by management
Assist with training, mentoring, and development of new employees, e.g. co-monitoring
University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
CRA II positions require 2+ years of clinical research monitoring experience

171

Senior Clinical Research Associate Resume Examples & Samples

University/college degree (life science preferred), or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from an appropriately accredited institution
In lieu of the above requirement, candidates with four (4) or more years of relevant clinical research experience in pharmaceutical, CRO industries or experience in a health care setting will be considered
Essential for candidate to have sound oncology experience

172

Clinical Research Associate Resume Examples & Samples

This position may also be at the Sr. or Prinicipal CRA level depending upon the selected candidate's experience and skillset
Demonstrate strong problem solving skills
BS / BA in a related scientific area
Minimum of 3-6 years of field monitoring experience
Medical device experience preferred, but not required

173

Clinical Research Associate Resume Examples & Samples

 Be primary point of contact for sites
 Build and maintain relationship with sites
 Monitor sites (Initiation Visits, Routine Visits, Close Out Visits, etc)
 Produce monitoring reports within SOP and monitoring plan timelines
 Coach investigators to be compliant with GCPs and the protocol
 Talk to site staff about site recruitment
 Ensure sufficient drug supply on site and reconcile drug on site
 Ensure high quality data and conduct at sites
 Identify and escalate issues or concerns to the internal Amicus team
 Identify, analyze problems and trends; provide and recommend solutions across studies
 Acts as liaison between CRO CRAs, Field Based CRAs and the PM
 Accountable for reviewing and approving all trip reports for assigned studies
 Develop training tools and training materials in support of the project
 Develop study tools for sites and CRA use
 Accountable for the quality of the trip report content
 Facilitate the review and provide input to the Monitoring Guidelines
 Co-monitor with 3rd party CRAs as needed
4+ years experience from similar work within a pharmaceutical company or CRO is preferable, but can also have experience as a research coordinator
Team player with a positive attitude
Self-motivated and able to function with little supervision
Highly detail-oriented
Superior communication skills, both verbal and written
Able to resolve conflicts in a diplomatic manner
Solid problem-solving and decision-making skills

174

Clinical Research Associate Resume Examples & Samples

Understanding of SOPs, WIs, FDA and local regulations as well as ICH-GCP guidelines
Demonstrates ability to prioritize and manage time for the preparation, completion and follow up of monitoring tasks
On site experience with most types of visits; PSSV, SIV, IMV, COV

175

Senior Clinical Research Associate Resume Examples & Samples

Thorough knowledge and application of project specific
Bachelor’s degree – Life Science preferred or
Consistently meets or exceeds metrics for quality trip

176

Clinical Research Associate Resume Examples & Samples

Assists with the review of protocols, informed consents, and study related documents
Maintains and tracks regulatory files/essential Master Documentation Files (MDFs) while working closely with other team members to ensure these documents are properly managed and are accurate
Interacts and supports internal and external personnel to facilitate meeting project timelines and tasks in accordance with Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) and all applicable regulatory guidelines
Supports Leidos CRAs and Project Managers with clinical site management
Assists with managing the relationship between Clinical Research Organizations (CROs) and field CRAs, as needed
Assists with investigator site activities in adherence to all applicable guidelines, including GCPs and SOPs
Ensures appropriate reporting of Adverse Events (AEs), Serious Adverse Events (SAEs) and unanticipated problems
Assists with the review and possible design and production of subject Case Report Forms (CRFs) and performing quality control on completed CRFs
Assists with clinical trials progress
Participates in and helps organize clinical trial activities with CROs, such as investigator meetings, study initiation, ongoing monitoring and close-out visit activities when applicable
Assists in preparation and production of documents for Food and Drug Administration (FDA) submission, as well as annual IND protocol reports
May assist in conduct of site visits and initiate draft reports and letters in a timely manner to ensure compliance with SOPs
May require local travel 5-10%
Possession of a Bachelor’s degree from an accredited college or university according to the Council for Higher Education Accreditation (CHEA) in a field related to biomedical research, clinical trials and/or health, or four (4) years related experience in lieu of degree
Ability to prioritize multiple tasks/projects through effective organization/planning skills
General knowledge of clinical trial fieldwork concepts and practices, FDA regulations and GCPs
Knowledge of database management
Must be willing to travel approximately 5 -10% local/domestic
Infectious diseases experience

177

Clinical Research Associate Resume Examples & Samples

Prior experience as a Clinical Research Associate
Must have demonstrated problem-solving abilities in overseeing clinical sites, and demonstrated tactfulness and diplomacy in dealing with study coordinators and physicians
Able to resolve routine issues independently
Knowledge of regulatory environment (ICH-GCP, relevant European and German laws)
Prior hematology / oncology clinical study experience
Driver’s license
MONEU

178

Clinical Research Associate Resume Examples & Samples

Provides clinical trials monitoring for NIAID and for a large network of clinical sites participating in Investigational New Drugs (IND) and non-Investigational New Drug (non-IND) protocols
Ensures sites are following U.S. Food and Drug Administration (FDA) regulations for INDs, Investigational Device Exemptions (IDEs), International Conference on Harmonization/Good Clinical Practices (ICH/GCP) guidelines, and other applicable regulations
Monitors the source documentation for the appropriate reporting of Adverse Events (AEs) and Serious Adverse Events (SAEs)
Critically evaluates clinical trial data for accuracy and completeness while ensuring the safety and confidentiality of participants
Provides assistance and monitoring of pharmacy records, including receipt, storage, labeling and final packaging, inventory, distribution and the processing and disposal of returned investigational agents according to the study monitoring plans and Standard Operating Procedures (SOPs)
Assists the Clinical Trials Management (CTM) team in maintaining relationships with site staff and/or network entities, Clinical Research Organizations (CROs) and field CRAs
Assists with the design, planning and implementation of clinical trials including protocol and Informed Consent Form (ICF) reviews
Coordinates project activities associated with monitoring functions of clinical studies for domestic and international sites and provides assistance to the clinical investigators and teams to reinforce and enhance a GCP culture
Conducts site study initiation, monitoring and close-out visits, completes reports in a timely manner
Ensures the conduct of the trial is in compliance with Standard Operating Procedures (SOPs) and GCPs, the approved protocol/amendment(s), NIAID Institutional Review Board (IRB) and NIH policies, and applicable regulatory requirements
Maintains Essential Documentation File contents, ensures accuracy and completeness of documents and reconciliation of the documentation
Assists other CRAs and Clinical Project Managers in working with investigators to generate and/or revise study-related documents
Assists with ensuring that the required approvals to initiate intramural research are in place
Assists in the preparation and production of documents for FDA submissions, as well as IND annual protocol reports and manuscripts
Reviews or helps create internal and/or external SOPs, guidelines and tools for the CTM team in support of NIAID staff
A minimum of two (2) years of progressively responsible experience in biomedical research including a minimum of one (1) year directly related to overseeing multiple concurrent trials
A minimum of one (1) year on-site clinical monitoring or site management experience
Ability to prioritize multiple tasks/projects, accomplish goals and meet expected timelines through effective organizational and planning skills
Ability to communicate effectively with non-technical and technical staff
Knowledge of clinical trial fieldwork, monitoring concepts and practices, FDA regulations and ICH GCPs
Proficiency with Microsoft Office products including Microsoft Word and Excel
Experience with electronic or remote data capture monitoring as well as paper based monitoring
Ability to travel approximately 30-40%
Must be able to obtain and maintain a security clearance
Familiarity with regulatory requirements and guidelines for clinical research, as well as monitoring requirements to ensure integrity of data and site compliance
Experience in the development of case report forms, manual of operations and study monitoring plans
Experience with database management such as TrackWise®
Ability to read French or Spanish

179

Senior Clinical Research Associate Resume Examples & Samples

To ensure that clinical studies are conducted at investigator sites in compliance with the current approved protocol and any protocol amendment(s), ICH GCP, GSK Written Standards and applicable local laws and regulatory requirement(s) so that the rights, safety and well-being of human subjects is protected and that the reported study data is accurate, complete, and verifiable from source documents
Fully accountable for ALL aspects of site management including ensuring completion and delivery of all local activities required to ensure high quality set up, execution and completion of studies. Ensure that critical study timelines related to monitoring activities are achieved and that recruitment targets, patient recruitment cycle times, data and audit quality and site related milestones are met. In addition to the monitoring duties of a CRA, the Senior CRA will demonstrate the ability to effectively manage multiple priorities and responsibilities of increasing scope and complexity
Communicate progress and relevant study information or escalate issues of the study to the local study management team and other key stakeholders e.g. CRA Manager
Responsible to contribute to the wider business by taking on leadership roles representing monitoring interests on internal and cross functional process improvement teams, standardizing processes, identifying and sharing best practices and continuous improvement
Act as a role model, coach, mentor for new or less experienced CRAs on processes, study, technical and behavioural competencies including resolving difficult situations
Build effective long-term collaborative relationships, and to uphold the reputation of GSK
Ensure the quality and integrity of clinical studies conducted in the LOC by taking on appropriate business management monitoring activities as agreed with local Quality and Training Manager
Provide training and monitoring support for new and less experienced CRAs, ensures competency of less experienced CRAs by participating in joint site visits or co-monitoring visits
Take a leadership role in standardizing processes within and across LOCs, identifying and sharing best practices and continuous improvement
Provide leadership in resolving complex monitoring issues through discussion with other CRAs, local study management and other GSK departments as appropriate
Performs operational site evaluation visits, study initiation visits, on and off site monitoring visits at the required frequency, and site closeout visits
At site evaluation visits, determines the feasibility of conducting protocols with reference to study complexity, staff availability, clinical facilities, potential for recruiting patients, site selection and ability to comply with ICH GCP investigator and GSK requirements for clinical studies
Deliver appropriate training to site staff and other relevant parties, as required. Assists with web based and face to face GSK trainings to ensure that investigators and site staff are appropriately trained in ICH GCP and study related procedures so that they can effectively run the clinical study
Participate in global investigators / monitor meetings as appropriate, facilitates investigator’s participation in global meetings and/or assist LSM with organising local investigator meetings
Participates in other study meetings as required
Assist the LSM / LCSS with site budget negotiation, the preparation of contracts and agreements with investigators, hospitals, pharmacies, labs, etc. using contract templates to run the studies in line with GSK and all regulatory requirements
Ensure that investigators and staff fully understand their roles and responsibilities with respect to regulatory requirements (ICH-GCP)
Completes monitoring visit reports within the agreed timelines
Accountable for tracking and managing study related payments to investigational sites
Ensure sponsor study records are inspection ready at all times and archives records as applicable
May take on role of local expert/champion or subject matter expert in a business system / process
Assists with audits/inspections of local clinical operations department & study /sites in the country
Acquire and maintain an appropriate level of knowledge on the pathology of disease area being studied, the study compound, the study protocol and all study related activities
Attendance at internal project meetings and relevant training courses. Participate continuously in relevant training courses to improve personal / professional skills
Keep up to date with all the changes / required knowledge on ICH GCP, GSK written standards and attending appropriate training sessions

180

Senior Clinical Research Associate Resume Examples & Samples

Ensure the fulfilment of objectives protocol conform concerning enrolment, patients , centres, timelines defined in the protocol (number of patients and centres, timelines
Ensure that ICH-GCP, corporate & local SOPs, and local regulations are respected and followed by all parties
4 years of CRA experience, at least 1 year of LCRA or CTL experience

181

Senior Clinical Research Associate Resume Examples & Samples

Advanced site monitoring skills
Advanced study site management skills
Advanced registry administration skills
Advanced verbal and written communication skills

182

Clinical Research Associate Resume Examples & Samples

Assists the trial manager in all aspects of trial development and initiation such as contract management, payment tracking, remote monitoring, study binder management and regular reporting to all active sites. Ongoing responsibilities to include
Ability to foster positive working relationships with a wide variety of internal and external personalities
Demonstrates a drive for continuous learning and continuous improvement
Balances an attention to detail with the overarching strategy
Knowledge of regulations governing clinical studies including GCP (Good Clinical Practices), PHRP (protecting human research participants), and HIPAA principles
Capable of learning new software packages as required
B.S. Degree in the health, life sciences, or engineering disciplines, or equivalent experience plus 3-5 years experience working in a clinical research environment, or an equivalent combination of education and experience

183

Clinical Research Associate Resume Examples & Samples

Monitors investigator sites to ensure the accuracy and validity of CRF entries in relation to patient records/clinic notes (source document verification). Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. Maintains regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Manages investigator payments
Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials
Manages the essential documents, as required by local regulations and ICH GCP, before, during and after a clinical trial
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System)
Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts
Maintains and completes administrative tasks such as expense reports and timesheets in a timely manner
Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members
Other project work as assigned
Basic medical/therapeutic area knowledge and understanding of medical terminology
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues

184

Clinical Research Associate Resume Examples & Samples

Unlike some CRA roles you will not be pushed to satisy unrealistic 'monthly visit' targets
Join a stable team of CRAs across Switzerland and benefit from outstanding training and development, both initially and throughout the year
Join a company where people tend to stay for 6-10 years rather than 1-3 years!

185

Clinical Research Associate Resume Examples & Samples

Monitor, track and manage all study related tasks at study sites ensuring compliance with GCP, ICH, applicable regulations and company SOPs
Requires a Bachelor’s degree (BA, BS or BSN) from a four-year college or university in a scientific discipline or equivalent combination of education and work experience
2 to 3 years of experience as a field based Clinical Research Associate required
Must be Bilingual (French and English)
Nursing or health care related experience helpful
Attention to detail and the ability to prioritize
Strong organizational, planning and follow-through skills. Ability to work well under pressure and with tight schedules. Self-direction and motivation are mandatory
Ability to exercise judgment within well- defined practices and policies for obtaining data
MS Word, Excel, knowledge of other presentation programs a plus
Must be able to travel with overnight stays both Domestic and Internationally

186

Clinical Research Associate Resume Examples & Samples

Consistently displays excellence in communication skills of a top level CRA
Exhibits ability to identify and interpret problems, recommend creative solutions, and influence appropriate changes
Demonstrates ability to effectively manage multiple priorities and responsibilities of increasing scope and complexity
Solid awareness of site dynamics and demonstrates ability to motivate, persuade, and educate site personnel

187

Senior Clinical Research Associate Resume Examples & Samples

Minimum of 5 years of clinical related experience, of which at least 3 years must be in clinical research monitoring
Strong site management and monitoring skills
Experience in multi-therapeutic areas desired
Excellent knowledge of regulations governing clinical research, ICH/GCP Guidelines and/or federal regulations, and applicable local regulations

188

Clinical Research Associate Resume Examples & Samples

Collaborates with Clinical Research Team to drive successful execution of global investigations
Assist in protocol feasibility analysis, country assessment, site identification, and patient recruitment and planning
Collaborates with Clinical Research Team to drive patient recruitment
Independently performs monitoring visits, including site qualification, study site initiation, routine monitoring and study site closure visits
Establishes and maintains regular contact with investigators, ethic committees, vendors and study sites to ensure legal compliance and assessment of accruals rates
Assists in investigation start-up activities including site selection and review of regulatory documents and ensures site is qualified for the study
Communicate project-specific information to/from trial sites and documents communication with investigations site/teams and escalate issues to team in a timely manner
Ensure the reporting of high quality data and timely query resolution
Maintain documentation for investigation sites as stipulated
Presents at and participates in investigator meetings, other study trainings and meetings as required
Maintaining current professional knowledge base of clinical research methodologies and FDA/EMEA requirements
Support statistical evaluation of study results within the clinical research department
Screening and identifying of business and product relevant scientific literature

189

Clinical Research Associate Resume Examples & Samples

Assumes accountability for individual role responsibilities as articulated by supervisor
Liaises with CROs and third parties related to the clinical study
Effectively manages time to meet project deliverables and deadlines in a manner that minimizes rework
Takes appropriate care to ensure quality of data
Keeps team and supervisor informed and up-to-date on information directly related to own position in the clinical operations study team
Minimum of college degree in a relevant discipline. Bachelors degree in relevant scientific discipline preferred
2-5 Years industry experience
On-site Monitoring

190

Senior Clinical Research Associate Resume Examples & Samples

Clinical Research responsibility for marketed products, product modifications and/or assigned new product programs (NPI)
Providing microbiology lab support to clinical programs
Preparation of clinical protocols, study documentation and clinical reports
Conducting study site feasibility assessments and qualification visits
Development and maintenance of claim sheets to support sales and marketing
Use knowledge to trouble shoot and investigate issues with assigned products and processes to provide resolution
Bachelor's degree or higher in a science related major from an accredited institution
Minimum of two (2) years microbiology laboratory experience
Minimum of four (4) years of clinical research experience
Master’s degree in science related field from an accredited institution
Certification as a clinical research associate (CRA)
Experience in one or more of the following areas: vascular access research, wound care research, skin research
Experience and knowledge of ICH and FDA guidelines
Experience working with customers in understanding/documenting voice of customer and user requirements
Excellent ability to multi-task and prioritize
Ability to work effectively on cross-functional teams

191

Senior Clinical Research Associate Resume Examples & Samples

Be responsible for all aspects of site management and monitoring activities for assigned applicable Phase I and all Phase II-IV clinical Investigator sites within the approved Clinical Development Plan (CDP). These global, complex studies are conducted within the standards set by Bayer Global Development, according to Good Clinical Practices (ICH - GCP) and applicable regulatory and legal requirements
Manage Investigator site and site activities and monitoring site data, to ensure patient safety and ethical and regulatory compliance necessary to provide quality data required for global regulatory submissions for approval of drugs
Manage Investigator sites to ensure the Investigator and Site Staff meet all aspects of study delivery and commitments to make certain the operational study execution is on track from site selection to site close out
Conduct Site Selection Visits to confirm the Investigator and Site Staff are qualified, and have suitable resources and facilities to properly conduct the study
Ensure completion of site documents necessary for ethics and regulatory approval for site initiation within agreed upon timelines. Ensuring all legal, regulatory and Bayer requirements are met prior to drug shipment to sites as well as all site initiation processes are completed
Ensure Investigator Agreements and budgets are negotiated and executed for assigned study sites, and subsequently initiating payments at key milestones
Train and supervise cross functional site personnel on study related procedures for the duration of the study
Bachelor’s Degree (or equivalent)
6 – 7 years of relevant healthcare experience including 4 years of monitoring & site management experience
In-depth knowledge of the drug development process including monitoring and site management, local and international regulations, ICH – GCP, drug safety requirements, data management processes and investigator grant parameters
Awareness and understanding of cultural differences as well as regional operational differences and budget management
Effective written and verbal English communication skills, strong oral presentation, interpersonal, decision-making and issue resolution skills are required
Effective planning and organization skills, attention to detail and excellent follow through

192

Senior Clinical Research Associate Resume Examples & Samples

Advanced degree or Bachelor’s degree in a biologic discipline with equivalent job experiences required; pathology or IVD experience preferred
8+ years of Clinical Trial Management experience for medical device, pharmaceutical or biological products; experience in diagnostics preferred
A solid understanding of clinical project management and familiarity with project management tools
Understand and have experience related to the regulatory requirements of China controlling bodies and framework as regards IVD development
Knowledge of pathology and/or oncology is necessary
Experience in working in parallel project teams
High work capacity is required at certain times in high priority projects
Experience in CRO/vendor management and contracting is preferred
The ability to organize and motivate others

193

Clinical Research Associate Resume Examples & Samples

Bachelor’s degree, preferably in a life science or scientific related field, or RN or BSN degree or 10+ years of recent and relevant clinical research/monitoring experience
Four year or more experience in clinical research, with a minimum of two to four years’ experience in independent coordination of investigational site activity by on-site monitoring and site communications
Intermediate knowledge and understanding of FDA regulations and ICH – GCP guidelines
Must work both independently and in a team environment
Proven track record of on-site monitoring of investigational sites and constructive site collaboration
Ability to review and interpret medical records through knowledge and general application of medical terminology
Excellent interpersonal, written communications, time management, and organizational skills
Detail oriented with good problem solving skills
Ability to manage multiple tasks and take ownership and workflow initiative
Proficient computer skills using Microsoft Office products
Experience with electronic data capture (EDC) is a plus
Presentation skills desired

194

Senior Clinical Research Associate Resume Examples & Samples

Managing and coordinating cross-functional project teams
Serving as the primary project contact with the Sponsor (Customer)
Monitoring team performance against contract, customer expectations, and project baselines
Leading problem solving and resolution efforts to include management of risk, contingencies and issue resolution
Developing study management plans, together with team assignments and accountabilities and oversight of database maintenance
Ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures

195

Senior Clinical Research Associate Resume Examples & Samples

Continuously assess site performance, processes, qualifications of staff, and suitability of facilities to ensure adherence to study protocol, Bayer Healthcare requirements, regulatory and local legal requirements, as well as ICH-GCP
Track to ensure sufficient resources at site to conduct study activities for duration of the study
Track enrollment activities to ensure site remains on track with site commitments and develop contingency plans to ensure site commitments are met
Review patient data at site to ensure safety of patient and patient data is consistent with what is reported in the case report form. Serve as liaison between Investigator and Study Medical Expert to resolve any medical patient-related queries. The data from these clinical sites are required to demonstrate patient safety and efficacy of investigational products which forms the basis of regulatory approval
Assure adequate control of investigational product (study medication), which includes: ensuring sites have met all local and legal requirements to receive investigational product, study drug storage, and continually ensuring patient compliance with expected study drug dosing. The Sr. CRA is responsible for study drug accountability at the site level and arranges for destruction of investigational product in accordance with local legal and regulatory requirements
Ensure applicable authorities are notified of study closure and final patient status in accordance with ICH and local regulations
Periodically review Investigator Site File to ensure essential documents are maintained according to ICH and SOP requirements
Understand that rigorous regulatory guidelines exist to ensure overall patient safety related to reporting of serious or unexpected adverse drug reactions. The Sr. CRA is responsible for training the Investigator and site staff on these strict regulations and procedures for timely reporting and as well as monitoring ongoing compliance. Strict adherence is essential to remain compliant with on time reporting from Bayer to regulatory authorities and critical for thorough and timely evaluation of patient safety
Proactively identifies potential issues and develops site Corrective Actions / Preventive Actions (CAPAs) Plans. The Sr CRAs ensures timely and sufficient resolution of issues that may impact compliance or quality of study related activities or data
Ensure essential documents are appropriate and filed in a timely manner in the Investigator Site File as this role is a key contributor to the Trial Master File and study documents at the country level
Be a key contributor in the preparation, conduct and follow up of Site Audits and Regulatory Inspections to ensure a successful outcome. The Sr. CRA is a member of the audit/regulatory inspection team
Be a mentor and role model for new or less experienced CRAs on process, study, technical or behavioral competencies. The Sr CRA may also conduct co-monitoring visits as defined in the Study Oversight Plan to mitigate risks and ensure the quality and reliability of study data and processes. In addition, the Sr CRA may participate in Expert Working Groups for Global SOPs, training or process improvement initiatives
Six (6) + years of relevant healthcare experience
Four (4) years of monitoring & site management experience
Effective written and verbal English communication skills, strong oral presentation, interpersonal, decision-making and issue resolution skills

196

Clinical Research Associate Resume Examples & Samples

Coordinate with study investigators to plan and implement new research projects
Assist with the design of data collection and tracking forms; develop and implement data tracking procedures
Coordinate and serve as the liaison with other research sites
Train and oversee data collection personnel; monitor quality assurance for data collection
Manage study databases with assistance from programmers and statisticians; produce data reports for tracking purposes
Perform other research related tasks, as needed
Bachelor’s required; Master’s preferred
Two to three years directly related experience; Certified Clinical Research Professional (CCRP)preferred
Strong organizational skills, attention to detail and responsiveness to deadlines
Ability to multitask, flexible, adaptable to change
Knowledge of research methodology
Ability to communicate effectively and tactfully with a variety of staff, faculty, researchers and business contacts
Experience with oncology trials
Word processing skills and familiarity with Windows-based software, Excel, Access, Power Point

197

Clinical Research Associate Resume Examples & Samples

Manage and oversee multiple research projects involving human subjects, particularly medical patients
Assist the Administrative Director with program planning, consenting of patients to research studies, IRB processing and compliance with federal, state, local and institutional research regulations
Manage research budgets and contracts
Supervise clinical research protocols and disease-related databases
Maintain a collaborative relationship with Principal Investigators and inter-departmental staff
May perform research project-related tasks such as subjects recruitment and data collection, as needed
Maintain and manage a tissue and specimen data bank for thoracic surgery and oncology
Two to three years directly related experience. Certified Clinical Research Professional preferred
Ability to communicate effetively and tactfully with a variety of staff, faculty, researchers and business contacts
Word processing skills and familiarity with Windows-based software, Excel, Access and PowerPoint

198

Senior Clinical Research Associate Resume Examples & Samples

Assists with the completion of activities regarding study execution; including working with functional areas and site monitors to ensure assigned activities are completed per plan. This may include assigned study region(s)
May have at least 1 year Pharmarelated
Demonstrates analytical and critical thinking skills
Possesses good communication skills

199

Clinical Research Associate Resume Examples & Samples

Identify potential investigators in collaboration with the sponsor
Perform evaluation visits to assess facilities and staff so as to ensure the selection of appropriately qualified investigative sites
Initiate clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted
Perform monitoring duties as specified in the relevant procedures
Verify data versus source documentation and validate CRF entries
Generate and resolve queries as required
Control investigational product accountability through physical inventory and records review. Control trial supplies ordering, dispatch, return and destruction, where applicable
As necessary, prepare and submit regulatory, ethics committee and provincial applications and regulatory packages
Ensure the proper essential documents are in place prior to trial start up and on an ongoing basis throughout the study - prepare Regulatory Compliance Review packages
Ensure administrative set up of sites, laboratories, storage facilities, equipment, etc
Organise and participate in investigator meetings as necessary
Provide trial status tracking and progress reports as required by the Project Manager or Clinical Team Manager
Administer investigator payments
Conduct and ensure proper trial close out and retrieval of trial materials
Archive relevant documents as per procedures
Clearly document all observations in reports and letters in a timely manner, according to accepted business writing standards. Ensure that any serious issues are immediately raised to the attention of project management, clinical team management and clinical operations management in writing
Maintain a working knowledge of GCP, Corporate global SOPs and applicable client SOPs
Facilitate effective communication between investigational sites and the PPD project team through written, oral and electronic contacts
Facilitate and respond to company, client and regulatory audits
Contribute to the project team by mentoring new members, assisting in preparation of project tools and sharing ideas and suggestions with team members
Bachelor's or higher graduate degree in a science related field, licensed or certified health care training or equivalent experience
Possesses a Valid passport
Knowledge and understanding of relevant regulations, e.g., ICH/GCP, FDA guidelines
Basic computer skills and the ability to learn appropriate software
Basic medical/therapeutic area knowledge and medical terminology preferred
Ability to travel and spend 60 to 80% of working week at site
A minimum of one to two years experience as a Clinical Research Associate / monitor or in a health sciences field / clinical research setting is required. Three years' experience for the Senior CRA role
LI-AP1

200

Clinical Research Associate Resume Examples & Samples

Under general supervision, follows established company policies and procedures and applies acquired job skills to…
Performs functions that require full knowledge of general aspects of the job
Works on assignments that are semi-routine in nature, but recognizes the need for occasional deviation from accepted practice
Contacts are typically with individuals within own department and occasionally with contacts outside own organization. Contacts involve obtaining or providing information or data requiring some explanation or interpretation
May provide assistance to A1 with more general support tasks that require a better understanding of functions, as directed by immediate supervisor
May refer to A3 for assistance with higher level problems that may arise
Escalates issues to supervisor for resolution, as deemed necessary
Review and comply with the Code of Business Conduct and all applicable company policies and procedures, local, state and federal laws and regulations
Utilizing defined guidelines and checklists, supports the FMS Clinical Studies Department CRO in the coordination, monitoring and tracking of clinical research studies, ensuring clinical activity receives appropriate Institutional Review Board (IRB) approval and is conducted in compliance with the designated protocol, the Office for Human Research Protections (OHRP), Good Clinical Practice (GCP) guidelines FDA regulations, and all applicable regulatory requirements
Collects essential regulatory and other study specific documentation related to the assigned project including up to date medical licenses, Curriculum Vitae, certificates and IRB approvals and ensures they are adequately filed and maintained
Ensures research activity has received all necessary IRB approvals
Verifies the investigator is following approved protocol and all GCP procedures on an on-going basis
Assists with PowerPoint training of investigative personnel on human subject protection, principal investigator obligations, GCP and local regulations to ensure sites are conducting clinical research according to protocol and regulatory requirements. Training may take place either at investigator meetings or at the investigative site
Works with investigational site staff on an on-going basis to ensure submission deadlines for safety reports and annual reports are consistently met
Manages the Trial Master File including the collection, review and ongoing maintenance of essential documents from Investigators, including ICF customization as well as the coordination of IRB submissions. Follows defined process/protocol to ensure the Trial Master File is ready for inspection by the FDA
Establishes a strong working relationship with sponsors and investigational sites serving as the in-house site management primary liaison, resource and main line of communication for the studies
Communicates effectively with investigational site staff maintaining a professional demeanor answering questions, investigating issues and triaging escalated issues as needed
Performs site selection visits for newly selected sites; follows established checklists to ensure sites have all of the necessary staff, materials, pill counters and appropriate locked cabinets
Works closely with study sites as needed ensuring Serious Adverse Events (SAE) are appropriately reported to the IRB in accordance with the study protocol and FDA regulations. Works with the Sponsor to ensure IND safety reports and alerts are distributed to all investigational sites and the CRO
Provides support in the preparation of on-site regulatory agency and/or study sponsor inspections and audits as needed. May need to travel on-site responding to identified issues providing documents, study specific guidelines, procedures and to answer questions demonstrating the study is in full compliance with established protocol, GCP and regulatory requirements. Works with investigative sites to ensure they are always audit ready
Creates and maintains clinical project documents including Monitoring Guidelines, Site Operations Manual and Monitoring Visit Letter templates under guidance of Project Manager/Clinical Team Lead/Director of Clinical Studies
Collaborates with site staff to ensure Case Report Forms (CRF) are completed accurately and consistent with source data
Assists with initial Investigator recruitment and evaluation by reviewing Site Feasibility Questionnaires and Investigator CVs. Final decision on Investigator participation is the responsibility of the study Sponsor
If necessary, may assist field CRA with verifying source data, clinical notes and other trial records are accurate, complete and adequately filed and maintained at the investigational site
Develops and maintains data collection/study tracking spreadsheets, tools and reports
Establishes and maintains a filing and tracking system for electronic and paper clinical trial files and documentation including Confidentiality Agreements, vendor payments, site contracts, and milestone payments to support monitoring activities
Assists with closing down investigative sites upon completion of the trial including essential document collection, transferring files to the sponsor or Iron Mountain and ensuring all unused trial supplies are documented and accounted for
Makes a continuous effort to keep abreast of regulatory and scientific developments by attending training courses and reading professional journals and publications
Facilitates trial-specific training according to industry standards for investigator and other site personnel and facilitates conferences for additional training as needed to ensure the successful conduct of the study
Occasionally attends face to face Investigator meetings to present training on CRF completion guidelines, study specific procedures, guidelines and drug accountability
Coordinates with the Sponsor, FMS Clinical Studies personnel and external customers to meet project specific goals including ensuring all sites are activated, have received IRB approval and study enrollment is on target to meet predetermined timelines
1 – 2 years’ related experience
Minimum of 2 years experience in clinical research
Clinical trials support or pharmaceutical industry experience preferred
Prior experience and proficiency utilizing computerized information systems and MS Office. Ability to develop and maintain Excel spreadsheets
Ability and willingness to travel up to 10% of time
Knowledge of ICH and drug and device regulations that are relevant to clinical trials preferred

201

Clinical Research Associate Resume Examples & Samples

Knowledge and experience in oncology trials is necessary
Knowledge of GCP/ICH guidelines
Ability to work independent to meet trial requirements and sponsor/contract deadlines
Proficiency with computer systems and Microsoft Office Suite (Outlook, Word, Power Point, and Excel) required
Attention to detail and demonstration of quick follow-up to study needs, commits to quality
Interpersonal skills and clear oral and written communication skills. Uses correct grammar, syntax, and format
Demonstrated adaptability, handles day to day work challenges confidently, is willing and able to adjust to multiple demands, shifting priorities; shows resilience in the face of challenges, demonstrates flexibility
Shows work commitment: sets high standards of performance; pursues aggressive goals and works efficiently to achieve them

202

Clinical Research Associate Resume Examples & Samples

Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing)
Conducts all clinical site monitoring activities according to the monitoring plan and in accordance with the study timelines and company objectives
Report monitoring activities and study site conduct accurately and completely. Prepare and submit written reports, both monitoring and administrative, in a timely, concise and objective manner
Proactively identifies issues that may impact enrollment and recruitment timelines, and provide objective comments regarding these issues. Collaborate with senior staff to develop initiatives and contingencies to ensure that timelines are met
Prepares CA and/or EC documentation, ensures submissions and/or notifications are performed as applicable. Manage and liaise with appropriate functions to respond to
CA and/or EC questions and related follow-up

203

Clinical Research Associate Resume Examples & Samples

Certified Clinical Research Professional (CCRP) or Certified Research Associate (CRA) OR acquired within two (2) years of hire
Human Research Subject Protection Course completion within three (3) months of employment
Experience managing complex data
Knowledge of Medical Terminology
One (1) year experience in health care field
Two (2) years administrative, data management or directly related experience in an acute care setting
Experience building and managing databases
Experience in Health Information Services
Competent in use of office software to include Word, Excel, Access, Outlook, and PowerPoint
Previous experience using Electronic Medical Records (EMR) such as EPIC

204

Clinical Research Associate Resume Examples & Samples

Analytical skills and ability to resolve problems
Working knowledge of data management programs
May assist with orientation and training of new staff
Minimum of 1-2 years of related experience OR completion of the CCPO New Staff Orientation program including completion of competency assessment

205

Clinical Research Associate Resume Examples & Samples

Plans, conducts, and completes investigations under the supervision of the Clinical Research Director
Assists with design and implementation of protocols utilizing vestibular equipment
Assists with the preparation of technical reports, summaries, and protocols

206

Clinical Research Associate Resume Examples & Samples

Implements and maintains the effectiveness of the Quality System
Complies with all policies, established procedures, and regulations related to clinical research
Actively participates as a member of the cross-functional project team
With direction performs the following: - Assesses data generated by R&D/Business Teams
Prepares design validation plans
Prepares documents for clinical studies
Proposes and negotiates budgets for clinical studies
Initiates payments to sites
Reviews data, prepares and presents clinical data reviews and data summaries
Responds to audits and data queries
Prepares the clinical sections of regulatory submissions and international registration packages
Assists Regulatory in preparing responses to regulatory agencies’ questions regarding the clinical study
Arranges for and assists in standard Statistical Support with the collection and statistical analyses of clinical data
Monitors standard clinical studies ensuring site compliance with the clinical protocol and ICH/GCP guidelines, assures subject rights, safety, and welfare is protected, ensures data integrity through completeness, accuracy, and legibility
Prepares and reviews product labeling and promotional materials
Conducts standard pre-study, initiation, interim, and close-out monitoring site visits and completes site visit reports. Initiates standard clinical studies and provides for investigator and staff training
Supports publication or presentation of clinical data in professional journals or meetings
Maintains professional, product, and market expertise via independent reading, networking, and training
Implements all policies, established procedures, and regulations into daily operations as appropriate
Develops professional, expertise via professional and educational opportunities
Assumes responsibility for attending training sessions, presentations, and continuing education sessions
Works with assistance to prepare publications, abstracts,or presentations for professional meetings
Contributes to goal setting
Takes responsibility for achieving results
Honors commitments
Accepts and completes all management-directed work assignments such as clinical assignments, travel, and other tasks
Demonstrates good basic writing skills. (i.e. clear, concise, effective, and well-organized) Demonstrates good presentation skills. (i.e. clear, concise, effective, and well-organized),Tries to understand changes in work tasks, situations, and environment as well as the logic or basis for change

207

Clinical Research Associate Resume Examples & Samples

Bachelor’s degree or above of Medical Science, e.g. medical, pharmacy, nursing, etc
Adequate English verbal and written skills
Requires a minimum of one year clinical trial experience within pharmaceuticals industry or Contract Research Organisation; preferably in clinical monitoring. Other experience may also be relevant, e.g. as study staff at a clinical research site
Knowledge of Good Clinical Practice (GCPs), International conference on harmonization (ICH) Guidelines, and local regulations, research process and scientific knowledge as relates to clinical trial conduct

208

Clinical Research Associate Resume Examples & Samples

Bachelor’s or Master’s Degree in a technical area such as animal science, biology, veterinary technology
Minimally two years of experience in a biological science area, a veterinary technician position, or research experience in an academic institution or the pharmaceutical industry
Excellent organizational and interpersonal skills and very good written and oral communication skills
Competence with multiple software platforms and data management experience
Desirable: Experience and interest in working with companion animals. Previous experience in a research environment (GCP/GLP) and/or previous experience in diagnostic testing. Experience with electronic data capture and remote communication tools and skills. Experience working with production and research facilities
Clinical study experience, data management experience
Ability to work well with colleagues at all levels of the organization
Ability to discern the appropriate communication type best to utilize given the situation at hand. For example, some colleagues can be helped over email or phone. Some require an office visit or Webex session to share the issues at hand
Patience to work through complex issues with colleagues in multiple locations
Strong Excel and Word skills

209

Clinical Research Associate Resume Examples & Samples

Functions independently in a clinical research setting and is responsible for the complete coordination of the Center for Childhood Cancer Research biorepository study
Will be expected to train, educate medical and clinical staff on the CCCR biorepository protocol and regulatory responsibilities, and interact directly with the investigative team
Responsible for CCCR biorepository research activities, including (but not limited to)
Informed consent process
Submission of specimens/data and confirmation that all requirements met
IRB submissions
Completing chart abstraction for initial data submission and clinical updates
Completion of data forms
Assisting with budget development
Coordinating obtaining specimens from central lab and transporting them for processing
Working with the informatics and lab management systems teams to design and improve data collection
Creation and editing of data collection forms
Maintain open and frequent communication with inpatient and outpatient clinical teams
Review sample information entered by the lab research assistant in lab management systems
Responsible for meeting enrollment projections within study specified time lines
This position will report to the CCCR Administrative Director of Research. and work closely with the Department of Pathology as well as leadership in the CCCR
Must be knowledgeable on, have full understanding of, and promote good clinical practices (GCP) and will be held accountable for adherence to all policies and procedures surrounding these processes and for maintaining up to date knowledge on these policies from IRB, FDA, ICH, GCP, or other sources
Provide leadership and direct responsibility for the implementation of study related activities
Oncology and/or pediatric clinical research experience preferred
Critical reasoning/problem solving skills to identify and resolve complex problems

210

Senior Clinical Research Associate Resume Examples & Samples

Manage Investigator site and site activities and monitor site data, to ensure patient safety and ethical and regulatory compliance necessary to provide quality data required for global regulatory submissions for approval of drugs
Manage Investigator sites to ensure the Investigator and Site Staff meet all aspects of study delivery and commitments and to make certain the operational study execution is on track from site selection to site close out
Six (6) years of relevant healthcare experience including 4 years of monitoring & site management experience

211

Clinical Research Associate Resume Examples & Samples

Minimum of 1 year experience with In Vitro Diagnostic (IVD) products
Experience in monitoring sites, excellent team skills, ability to prioritize and multi-task in a fast-paced environment
Experience in the handling and shipping of Biohazardous specimens
Familiar with clinical literature in field of study and related areas

212

Senior Clinical Research Associate Resume Examples & Samples

Works under moderate guidance and participates in the planning and implementation clinical research projects; contributes technical and clinical operations expertise
May coordinate the activities of relevant colleagues within the Company and investigators to ensure compliance with the overall scientific study objectives. May work with international investigators and key customers as well
Travels to field sites to monitor studies
Under moderate guidance; plans and prepares studies
Manages training and coordinating certification of study site personnel
Ensures site compliance with regulations and study protocol
Monitors the sites and provides technical assistance, as necessary
Manages material logistics for the studies
Organizes investigator meetings, as necessary
May act as a lead for assigned projects and/or Project Team Meetings
Evaluates and escalates decisions impacting project team and/or work area(s) and/or broader organization
Maintains a high level of professional expertise through familiarity with scientific literature, Company product portfolio, and competitve environments
Processes and applies specific knowledge to the completion of difficult work assignments

213

Clinical Research Associate Resume Examples & Samples

Field monitoring of studies and data collection for clinical trials with increased volume and moderate complexity, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements
Provide oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, study sponsor management and leadership staff, including Institutional Review Boards/Ethics Committees/Research Ethics Committees, Clinical Operations (e.g. Contracts), and recommend and develop basic process improvements
Develop and deliver training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities
May edit/amend informed consent documents
Bachelor’s degree and 3 years previous industry clinical research experience OR Associates degree with 5 years previous industry clinical research experience
Experience with electronic data capture preferred
Moderate knowledge and understanding of Edwards policies, procedures, and international and domestic medical device regulatory guidelines relevant to clinical studies
Moderate understanding of cardiovascular anatomy, pathology and physiology or Business Unit area of expertise
Advanced proficiency in Microsoft Office Suite, including Word, Excel, and PowerPoint and electronic data capturing system (e.g., iMedidata)
Excellent written and verbal communications skills
Advanced problem-solving skills
Strict attention to detail
Ability to interact professionally with all organizational levels
Ability to manage competing priorities in a fast-paced environment
Ability to work in a team environment, including inter-departmental teams and representing the organization on specific projects

214

Clinical Research Associate Resume Examples & Samples

Conduct study feasibility assessment activities (if applicable)
Develop key study plans and manuals as per the study team / project team charter
Develop of critical study documents, such as study protocol, eCRF, ICF template, and others
Identify CLO risks and mitigations and aligning with cross-functional Study Team on overall Risk
Contribute to vendor evaluation and selection process
Conduct day-to-day management of CRO and vendors’ contracted activities as per oversight plans
Ensure final payments to vendors at study closure
May collaborate with other functions as needed to support execution of CLO cross-functional activities, such as: user requirement specification review (IXRS, Global Labs, Specialties Labs), user acceptance testing, and data review
Coach and mentor CTAs
Determine clinical supply requirements, including ancillary supplies and comparator drugs
Ensure compliance with ICH, GCP, SOPs during the execution of the study
Contribute expertise to functional and cross-functional process improvement activities, as needed
Execute on TMF maintenance
3-4 years of pharmaceutical industry or relevant experience
2 years of experience in a CRA functional role

215

Associate Clinical Research Associate Resume Examples & Samples

With support, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites
Develops strong site relationships and ensures continuity of site relationships through all phases of the trial
Minimum of 2 years of clinical research experience (i.e. Clinical Trial Assistant, Study Coordinator, Regulatory Clinical Trial Coordinator or similar)
Oncology Therapeutic Area experience
Fluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand technical information. Developing ability to present technical information with support
Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines
Hands on knowledge of Good Documentation Practices
Developing skills in Site Management including management of site performance and patient recruitment
Developing level of monitoring skill and independent professional judgment
Good IT skills (Use of MS office, use of some clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices
Effective time management, organizational and interpersonal skills, conflict management
Able to work with other experienced research professions to develop skills across multiple protocols, sites and therapy areas
High sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment, with support from Line Manager
Works effectively in a matrix multicultural environment. Ability to establish and maintain culturally sensitive working relationships

216

Clinical Research Associate Resume Examples & Samples

Participates & provides inputs on site selection and validation activities
Performs remote and on-site monitoring & oversight activities using various tools to ensure
Minimum of 2 years of direct site monitoring experience in a Biopharmaceutical, Pharmaceutical or CRO company
Travel: 65%-75%
Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines
Ability to understand and analyze data/metrics and act appropriately
Effective time management, organizational and interpersonal skills, conflict management, problem solving skills

217

Clinical Research Associate Resume Examples & Samples

A general familiarity with clinical trials research processes
Previous related experience in research within a clinical or corporate setting or relevant clinical experience in a clinical/hospital environment
Certification as a Research Professional by Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP)
Work habits include organization, coordination of many tasks, accuracy, and attention to detail

218

Clinical Research Associate, Melbourne Resume Examples & Samples

Responds to company, client and federal regulatory requirements/audits
Ability to attain and maintain a working knowledge of GCPs and applicable SOPs
Ability to remain flexibile and adaptable in a wide range of scenarios

219

Senior Clinical Research Associate Resume Examples & Samples

Able to work within teams and independently
Ability to effectively manage multiple priorities and responsibilities of increasing scope and complexity
Strong planning & organizational skills, and the ability to work efficiently and effectively in a dynamic environment
Recognizes potential obstacles and works to resolve them within set timelines, takes responsibility for own actions
Respects confidentiality in terms of PII
Proactive, conscientious and precise in delivery of quality work even when under pressure
Effective at analyzing and escalating issues, solving problems and resolving conflicts in a timely manner
Flexible with high learning and change agility
Knowledge of local regulations, IND/ICH GCP - guidelines, GSK written standards
Available and willing to travel as job requires
Strong computer skills with good eye for detail
Acts as role model in line with GSK core values and behaviors

220

Clinical Research Associate Resume Examples & Samples

Develops professional expertise; applies company policies and procedures to resolve a variety of issues
Utilizes defined guidelines and checklists, supports the coordination, monitoring and tracking of clinical research studies, ensuring clinical activity receives appropriate Institutional Review Board (IRB) approval and is conducted in compliance with the designated protocol, the Office for Human Research Protections (OHRP), Good Clinical Practice (GCP) guidelines FDA regulations, and all applicable regulatory requirements
Assists with PowerPoint training of investigative personnel on human subject protection, principal investigator obligations, GCP and local regulations to ensure sites are conducting clinical research according to protocol and regulatory requirements
Organize and manage Investigator Meetings and study Kick Off Meetings. Ensure all participants are reimbursed for any expenses incurred
Actively manages studies in Clinical Conductor Enterprise (CCE).This may include tracking CDAs, site contracts and milestone payments
May be required to attend face to face Investigator meetings to present training on CRF completion guidelines, study specific procedures, guidelines and drug accountability
Coordinates with the Sponsor, personnel and external customers to meet project specific goals including ensuring all sites are activated, have received IRB approval and study enrollment is on target to meet predetermined timelines
Be available by phone to study Sponsor evenings and weekends when study Project Manager is unavailable
May provide assistance to junior level staff with general tasks that require a better understanding of functions, as directed by immediate supervisor
Assists with various projects as assigned by direct supervisor
2-5 years’ clinical research experience; or an advanced degree without experience; or equivalent directly related work experience
Prior experience and proficiency utilizing computerized information systems and MS Office

221

Clinical Research Associate Resume Examples & Samples

Life Plans
Disability Plans
Voluntary Benefits Plans

222

Clinical Research Associate Resume Examples & Samples

You have a bachelor’s degree or higher in medical science or other relevant degrees
You are a strong communicator with a high level of energy and the ability to handle different priorities at the same time
You have good understanding of current International Council on Harmonisation - Good Clinical Practice (ICH-CGP) and local requirements of clinical research
You are able to create strong internal and external relationships and to drive positive team-spirit
You come with a “can-do-attitude” and a structured approach to problem solving
You are fluent in both written and spoken of English and Bahasa Malaysia at a professional level
You are open to travel within Malaysia approximately 3 times a week

223

Senior Clinical Research Associate Resume Examples & Samples

Thorough knowledge and application of project specific protocol
Consistently completes travel scheduling in accordance with project specific and UBC guidelines
Consistently completes site monitoring reports, confirmation/follow-up letters per UBC and/or client SOPs; signs, scans and/or provides to Clinical Site Specialist/Regulatory Document Specialist for filing in Trial Master File according to UBC and/or sponsor timelines requiring minimal corrections
Enters site visits, confirmation/follow-up letters and site monitoring reports into UBC’s Clinical Trial Management System
Monitors within Electronic Data Capture data entry, if applicable, and assists sites with Case Report Form resolution
Completes Regulatory Binder and Investigational Product reconciliation
Thorough knowledge of International Conference on Harmonisaton, Good Clinical Practice guidelines, Code of Federal Regulations and UBC SOPs

224

Senior Clinical Research Associate Resume Examples & Samples

Responsible for providing coordination and support to all clinical operation team to ensure achievement of study goals, as well as tracking and maintaining study logistic information, systems and tools and appropriate study documentation in order to improve and maintain the quality and effectiveness of processes and activities in clinical operation in accordance with ICH GCP (Good Clinical Practice), local regulations, timelines and Company’s Standard Operating Procedure (SOP)
Conducting activities related to start-up, on-going and close down phase. Including delivering training, site management, monitoring and support
Ensuring management of invoices and payments including assisting as well as maintaining study payment trackers in Quantum
Reconciling and tracking essential documents for the country level Trial Master File (paper or electronic) according to ICH-GCP and Roche procedures. This may include collection/retention/reconciliation of regulatory and investigator documentation, safety reconciliation, drug and non-drug reconciliation
Ensuring documentation and archiving for all clinical study documents as per required in ICH –GCP, Roche SOP and Local Regulations
Organizing and coordinating the logistic of internal and external meetings. These includes team meeting and external meeting, Investigator meetings
Becoming co-monitor, as required and with appropriate oversight and training, during high volumes periods (eg. initiation visit, document reconciliation at study close-out) or when appropriate, to alleviate back logs in study workload which could potentially have a negative impact in achieving project
Developing and maintaining functional knowledge of GCPs, Roche SOP and Local Regulations and therapeutic area (s) through continued training provided by APT or other function to ensure patient safety and data integrity

225

Senior Clinical Research Associate Resume Examples & Samples

Project manage all clinical trials, studies, limited market release projects responsible for
Initiates writing of all study related documents and gathers feedback from cross functional teams
Assists in writing and developing clinical protocols, data and tracking forms, informed consent documents, and clinical report forms
Monitors and tracks patients at clinical sites
Data collection of clinical research cases
Track data report forms, reports, and documents necessary for completion of clinical study, both in-house and from participating study sites
Assists in writing annual and final clinical study reports
Ensures accurate, up-to-date records of all documents and protocols of all clinical studies
Ensures the effective fulfillment of objectives and deadlines assigned to the group
Participate in proactive team efforts to achieve departmental and company goals
Generate basic analysis of data and provide data analysis to outside consultant or internal Align Statistician
Travel may be required – up to 40%
Bachelor’s degree in Science or equivalent years experience
2-5 year experience as a Clinical Research Associate
Highly recommended: Some orthodontic/dental knowledge
Ability to give presentations and updates on clinical research
Greater independence
Limited supervision
Ability to work on projects with limited training

226

Clinical Research Associate Resume Examples & Samples

Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs Good planning, organization and problem solving abilities
Ability to work with minimal supervision Good communication and interpersonal skills
Fluent in English and Spanish, both written and verbal

227

Clinical Research Associate Resume Examples & Samples

Four years of direct experience in clinical biomedical and/or behavioral research required
Must possess a current Tennessee State Board of Nursing license if primary residence is Tennessee or a Nurse Licensure Non-Compact state
Must possess a current State Board of Nursing license in the state of primary residence if the state is a Nurse Licensure Compact state

228

Clinical Research Associate, Istanbul Resume Examples & Samples

Determine protocol and regulatory compliance at the sites
Life science degree – Pharmacy, Biology or other related
In-depth understanding of ICH/GCP guidelines
Experience with Oncology, Hematology or infectious diseases
Excellent standard of verbal and written communication skills in English and Turkish languages
Good organizational skills with strong attention to detail and deadlines
Advanced skills across all of the Microsoft packages

229

Senior Clinical Research Associate Resume Examples & Samples

Perform on-site and remote monitoring and study closure activities across multiple protocols in a therapeutic area
Proactively drive project success, including collaborating with cross-functional team members
Ensure that sites operate in compliance with study protocols, SOPs, ICH/GCP guidelines, and Federal Regulations
Interact with study management teams, Sponsors, and additional CRAs involved in projects

230

Clinical Research Associate Resume Examples & Samples

Develop and maintain the department’s ability to produce infectious pathogens such as (but not limited to) human and rodent malaria, leishmania, dengue virus, and Zika virus. All tasks apply to production of any such pathogen, most of which are propagated concurrently within the lab
Continually maintain parasite life cycle in animal models and mosquitoes or sandflies, to include multiple parasite species and strains maintained concurrently, resulting in hundreds of plates, flasks, and infected animals needing attention each day, depending on demand. Maintaining these cultures might require working weekends based on the number of cultures in process and external requests. The contractor will endeavor to improve efficiency, capability or capacity of new and existing culture methods and will keep abreast of current and emerging literature concerning parasite/viral propagation and culture
Prepare vectors for infectious feeds and infect vectors using appropriate feeding devices, direct animal feeds, or injection methods. Feedings/injections will occur multiple times a week, sometimes several times a day, and sometimes on weekends, depending on demand. The contractor shall communicate with supervisors and other personnel to determine demand and adjust production and schedule accordingly
Cultivate and continually maintain parasites, viruses, etc. in tissue culture and maintain laboratory records of parasite/virus growth and differentiation. The contractor will monitor parasite/virus development in infected vectors and in vivo animal infections by dissection and microscopic examination or molecular techniques, as appropriate, and maintain laboratory records of parasite/viral development and propagation
Provide a final project record and report which shall include written reports, data summaries, troubleshootedand maintained databases, published research findings in peer-reviewed journals, and presented research findings at scientific meetings and conferences
Be familiar with all cell culture, microbiological, molecular and other applicable techniques and methodology, Biological Safety Level 2 safety procedures, use of laboratory personal protective equipment, be familiar with WRAIR safety standard operating procedures (SOP), and attend WRAIR annual safety courses and other training, as offered
Independently plan, execute and analyze basic research studies on the in vitro and in vivo cultivation of all parasite stages, viral propagation, vector-pathogen interactions, transmission biology and other applicable avenues of scientific investigation
Assist in the preparation of infected vectors and execution of challenges for CHMI clinical trials according to protocol, schedule, and applicable regulatory governance
Assist with the preparation and stewardship of laboratory reagents, methodology, equipment, biological materials and other materials pertaining to experiment execution and laboratory cleanliness and safety
Work collaboratively to achieve the above. May require working evenings and weekends
2-5 years of related experience in scientific research, analysis and/or engineering
Knowledge of developing and conducting experiments involving high complexity assays
Understanding of microscopic examination of specimens, preparation of laboratory reagents, sterile techniques, and basic tissue culture techniques

231

Clinical Research Associate Resume Examples & Samples

Assist with the study site selection process by preparing feasibility questionnaires and conducting site interviews by phone
Develop various study specific forms/templates and prepares/ manages study status reports. Assist in vendor set-up, and oversight of vendors (including clinical CROs)
Review essential documents from study sites for accuracy and completion
Request set-up of TMF and review for reconciliation of required documentation
Primary contact for coordination of protocol questions from CRAs and study sites: Answering purely administrative protocol questions according to level of experience
Communicates all relevant and critical issues to management
Maintains close liaison with research coordinators at clinical sites
Assures compliance for assigned projects with clinical research policies and procedures
Reviews study and investigator budgets
This role is part of a career path advancing from CRA levels into Clinical Project Management over time
Has ability to understand the disease under study and the aim of the therapy. Should be able to understand the relevant sections of the study protocol
This position requires a sound knowledge of computer business software and meticulous attention to detail
Monitoring experience is a plus

232

Senior Clinical Research Associate Resume Examples & Samples

Plans, implements and executes FDA registration studies to support clinical claims
Supports the preparation of reports and summary documents (for internal and external customers) for product registration
Assists team in budget and contract negotiations with study sites, central laboratories and CROs. Monitors adherence to the study budgets and timelines
Conducts study start-up, monitoring and study close-out visits
Ensures adherence to regulations, guidelines and departmental standard operating procedures
Plans and prepares execution of studies through all phases of the study process
Provides technical input to study designs and clinical development plans
Reviews study protocols, reports and manuscripts
Works with Data Management and Biometrics staff on the design of documents and processes for the collection of study data from participating sites
Ensures study site compliance with Good Clinical Practices, regulations, SOPs and protocols
Ensures accurate and complete study management/data collection and transfer into the data management system
Acquires and maintains technical knowledge of product line

233

Senior Clinical Research Associate Resume Examples & Samples

Function as a research study project manager
Participate in planning of company’s research studies
Participate in writing study protocols and supporting documents, including case report forms and patient consent templates
Participate in study site and investigator selection and qualification processes
Represent company in interactions with institutional review boards for initial submission, continuing review, and regulatory reporting
Manage preparation of the investigator binders, case report forms and other documentation required for the conduct of the clinical trial
Manage setting-up study sites, which includes ensuring each site has the trial materials and training site staff on study protocols
Develop monitoring and patient recruitment plans
Monitor studies—visiting the study sites as needed
Directly interact with investigators, study site personnel, and CRO personnel
Verify that data entered onto CRFs are consistent with patient clinical records (source documents)
Communicate with study site personnel to resolve data queries
Collect completed CRFs from study sites
Write and submit site visit reports and letters
File trial documentation and reports
Ensure accountability of study articles
Close study sites as needed
Archive study documentation and correspondence
Communicate with company’s senior research personnel concerning problems and other relevant issues
Bachelor’s degree in scientific discipline
Ten years clinical research experience is preferred
Five years clinical trial monitoring experience is preferred
Certification as a Clinical Research Associate is preferred
Experience working in medical device industry is preferred
Familiarity with Good Clinical Practice guidelines, FDA requirements, and ICH guidelines
Ability to multitask, manage multiple deliverables, and meet strict deadlines
Knowledge of Microsoft Office programs, including Word, Outlook, Excel, and PowerPoint

234

Clinical Research Associate Resume Examples & Samples

Conducts routine and for-cause quality assurance and monitoring activities (with the exception of investigator-held IND/IDE studies) and clearly documents findings related to work performed
Minimum of 3 to 5 years relevant work experience in study coordination, research compliance, and/or conducting monitoring or quality assurance audits in the research setting
Equivalent combination of relevant education and/or experience acceptable
Demonstrated knowledge of applicable federal, state and local regulations and guidance documents, pertaining to research compliance

235

Clinical Research Associate Resume Examples & Samples

Ensure that studies are correctly designed, coordinated, completed and analysed to provide the highest level of scientific evidence and more effective outcomes
Develop and review trial protocols including literature searches of published articles
Coordinate communication with the ethics committee and study sites, including completion of ethics application and associated governance documents
Study planning and management of plan execution, in accordance with global study metrics
Design the layout for data collection forms
Setting up study sites, monitoring trials and closing down study sites
Training of and liaison with clinical study personnel
Budget preparation and reporting
Verifying data
Writing site monitoring visit reports
Assisting preparation of and reviewing manuscripts for journal submission
Hold regular update meetings and information sessions with marketing divisions on clinical studies
Communication of trial activities to internal stakeholders
Experience in Clinical Research in a similar medical environment
Completed tertiary qualifications in science, allied health or a related field
Exposure to clinical trials
Be self-motivated and have the ability to work autonomously and within a team
An attitude that thrives on achievement and in getting things done

236

Clinical Research Associate Resume Examples & Samples

Minimum of three (3) years combined clinical research, biomedical and/or medical device industry experience (academic clinical research experience is considered qualifying)
Bachelor’s degree or higher in Electrical Engineering or Mechanical Engineering from an accredited institution
Experience working in hospital or clinical setting or medical laboratory
Experience and knowledge of International Conference on Harmonisation (ICH) and FDA guidelines
Ability to multitask and think on your feet
Numeracy and attention to detail
Ability to work effectively on global cross-functional teams

237

Clinical Research Associate Resume Examples & Samples

2 +years of laboratory experience in molecular biology assays
Basic computer skills in MS Word, Excel and Outlook
Associate or Bachelor's Degree

238

Senior Clinical Research Associate Resume Examples & Samples

Leads the conduct and oversight of clinical and human factor/ergonomic studies. Studies may be conducted as either Investigator Initiated or Sponsor initiated studies
Responsible for compliance with procedures, federal regulations, and standards of Good Clinical Practice
Maintains required documentation for studies including values for annual transparency reporting
Performs scientific literature searches as needed to support team members
Performs technical and medical writing; periodically author Clinical Evaluation Reports and White papers in addition to study protocols and reports
Reviews and provides feedback on collateral material in development
Support other objectives as needed for the clinical research department (i.e., procedure development)
Contributes to the design of clinical studies
Maintains familiarity with scientific literature, product portfolio and competitive environment
Travels to clinical sites and conferences to meet with study Investigators and oversee clinical studies
Reviews study protocols, reports and manuscripts. Contributes technical and clinical operations expertise for these documents
Manages study inventory logistics and inventory tracking for studies
Responsible for management of day to day activities of outsourced clinical site activities, including ensuring vendors meet related deliverables
Maintains expertise in regulations for various types of studies (IDE, non-significant risk, feasibility, exempt, etc.) and serves as a resource related to clinical trial regulations
Participates in site selection, qualification, study initiation, interim monitoring and closeout activities
Ensures appropriate communication within and across functional groups
Assist in the development of site budgets and may assist in budget negotiations
Oversee clinical sites, partnering with monitors and site staff to identify and escalate or resolve compliance issues. Communicate any need for corrective action at sites
Prepare and/or review trial-related documents including but not limited to Informed Consent Forms (ICF) and Case Report Forms (CRFs), site specific documents (informed consent template and study tools/worksheets), investigator contracts, and study milestone documentation
Potential exposure to blood borne pathogens and other potentially infectious materials

239

Senior Clinical Research Associate Resume Examples & Samples

Accountable for execution and oversight of local operational clinical trial activities for assigned protocols in compliance with ICH/GCP and country regulations, client policies and procedures, quality standards and adverse event reporting requirements internally and externally
Ownership of country and site budgets; development, negotiation and completion of Clinical Trial Research Agreements; oversight and tracking of clinical research-related payments; payment reconciliation at study close-out; oversight and maintenance of financial systems
Responsible for execution and oversight of clinical trial country submissions and approvals for assigned protocols; development of local language materials including local language Informed Consents and translations; interactions with IRB/IEC and Regulatory Authority for assigned protocols
Responsible for managing country deliverables, timelines and results for assigned protocols to meet country commitments; responsible for quality and compliance in assigned protocols in country; contribution to the development of local SOPs; overseeing Clinical Trial Coordinators as applicable
Coordinates and liaises with Country Research Manager, Clinical Trial Coordinator, Clinical Research Associate, (Finance and Legal if appropriate) to ensure country deliverables are obtained for submissions, budgets, Clinical Trial Research Agreements and local milestones; collaborates closely with Regional Operations to align country timelines for assigned protocols
Oversight and coordination of local processes; clinical and ancillary supplies management, im- and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention requirements, and insurance process management; enters and updates country information in clinical systems
Bachelor's Degree (or comparable) in Business Finance/Administration/Life Science or equivalent Health Care related experience
Requires expertise of core clinical systems, tools and metrics
Excellent English skills required
Strong coordination and organizational skills required
Position requires extensive experience in clinical research operations and experience with project management and coordination
Expertise of core clinical, regulatory and financial systems, tools, metrics and local requirements is essential
Strong communication, leadership, and negotiation skills as well as excellent influencing and training/mentoring skills, both written and verbal, in local language and English
The ability to focus on multiple deliverables and protocols simultaneously is essential. Requires that the individual has ability to work effectively also in a remote virtual environment with a wide range of people
Ability to pro-actively identify issues and risks, analyze root cause, and propose solutions to problems and escalate to management as applicable

240

Clinical Research Associate Resume Examples & Samples

Baccalaureate degree or equivalent experience with courses in public health, community program development, psychology/sociology, and research
Valid driver’s license at time of hire
Proficiency in Microsoft Word, Internet, Excel, and e-mail
2 years of research or data entry/registry experience
Registration: Clinical Trials Management Certification
Understanding of GCP and ICH regulations, clinical trial monitoring, and regulatory compliance
Experience in oncology
Experience with Electronic Data Capture (InForm, Medidata Rave, etc.) systems
Experience with medical terminology, tumor registries, or clinical research

241

Senior Clinical Research Associate Resume Examples & Samples

The SCRA conducts clinical site monitoring visits across a maximum of 5 protocols and multiple therapeutic areas, ensuring AbbVie studies are conducted according to all applicable regulations and business processes
Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members
Appropriately reports and escalates serious or outstanding issues to project team member(s) and/or ACOM/COM/ Sr COM as appropriate, as defined in the study monitoring plan
Facilitates Quality Assurance Audit processes as indicated. Ensures regulatory inspection readiness at assigned clinical sites
Collaborate with senior staff to develop initiatives and contingencies to ensure that timelines are met
Prepares CA and/or EC documentation, ensures submissions and/or notifications are performed as applicable. Manage and liaise with appropriate functions to respond to CA and/or EC questions and related follow-up
Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators
Participates in departmental and other functional meetings as needed, including Site Management & Monitoring meetings
Identifies and partners with other AbbVie personnel to develop innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations while conserving overall departmental operating costs
Maintains knowledge and expertise across multi-therapeutic areas through clinical and scientific literature review, ongoing awareness and trends of industry practices and participation in professional activities
Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations
Good written and verbal communication skills. Written and verbal fluency in English and local language (if not English)
Acute observational skills, analytical and conceptual capabilities
Ability to work independently with minimal supervision

242

Clinical Research Associate Resume Examples & Samples

1) Implements assigned research studies by reviewing study and assessing institutional requirements
14) Maintains courteous and effective interactions with colleagues and patients
15) Demonstrates an understanding of the job description, performance expectations, and competency assessment
16) Demonstrates a commitment toward meeting and exceeding the needs of our customers and consistently adheres to Customer Service standards
17) Participates in departmental and/or interdepartmental quality improvement activities
18) Participates in and successfully completes Mandatory Education
19) Performs all other duties as needed or directed to meet the needs of the department. Qualifications Education: Associates degree or equivalent work experience

243

Clinical Research Associate Cra-norway Resume Examples & Samples

Willingness and ability to travel
Excellent English/Norwegian skills
Previous experience in the CRO industry would be advantageous

244

Clinical Research Associate Resume Examples & Samples

Perform data entry, collection, and analytics to be utilized in programs across Hanger
Assist with literature reviews with direction and supervision
Assist in the preparation of both grant and IRB submissions with direction and supervision
Maintain databases to be used by multiple teams
Able to interface in person and electronically with both internal and external clinical, administrative and executive personnel
Respond to project related communications proactively and timely
Provide administrative and data support to clinical teams by assisting project teams in the completion of assigned project activities
Attend project meetings as required
Assist with travel arrangements
Exhibit good written and verbal communication skills
Critical thinking skills
Demonstrate basic knowledge in mathematics, statistics and sciences
Basic understanding of the orthotic and prosthetic profession
Basic knowledge of MS Office suite programs
Demonstrate high ethical standards regarding confidential patient information
Typically requires less than 1 year of related experience

245

Senior Clinical Research Associate Resume Examples & Samples

If assigned; Responsible for identifying training needs and standardizing and facilitating training solutions for SMM monitors globally. Provide consistent best practice approach to onboarding, consolidating "lessons learned" across areas and incorporating into monitoring training materials, defining best practice training curriculum, and maintaining awareness of upcoming changes to ensure effective training is delivered in a timely manner
If assigned; With guidance, may serve as key point of contact in country/district for assigned study. Update Impact/Tesla with country-level information: Country-level planning timelines, LSR assignments
Site Monitoring Experience: Minimum 3 years

246

Senior Clinical Research Associate Resume Examples & Samples

BA/BS or higher in nursing, life or health sciences is preferred
5 years of pharmaceutical industry experience
4 years of experience in a CRA functional role
Experience mentoring CRAs and CTAs is preferred
Strong preference given to those with industry experience (pharma/biotech)

247

Clinical Research Associate Resume Examples & Samples

Prepares and completes critical study documents and performs final editing/proofing prior to publishing (e.g. protocol; synopsis; flowchart; informed consent template; investigator brochure; monitoring guideline; statement of work laboratory, other vendors, and CROs; consultant agreements; investigative device/drug labels; clinical study worksheets; etc.)
Monitors resources/reports to deliver milestones on time and budget
Collect, reviews and files all clinical study documentation for assigned trial(s) and investigative sites and maintenance of clinical trial master file (CTMF): assures all documentation is maintained in compliance with all applicable guidelines and corresponding SOPs
Participates, with the CTM, in the preparation and hosting of clinical study team meetings on an established schedule, providing agenda, recording/distributing of minutes and copying of minutes to CTM
Works with the CTM to prepare and compile materials for clinical study conduct and reference information for study sites provided to the site in the form of an investigator site file (ISF)
Prepares, collects and archives all study related correspondence to the investigator site including, but not limited to, newsletters, “Dear Dr.” letters, FDA/HA correspondence, contractual agreements and others
Responsible for investigator recruitment and maintaining current contact information for each assigned investigator site, as well as preparing investigator site file for participation approval
Collects pre-study documentation and essential regulatory documents from assigned investigator sites, as well as, collects updated documents prior to study initiation and on an ongoing basis
Estimates, orders and coordinates shipments of clinical study supplies to assigned investigator sites
Assists the CTM with tracking and requesting grant payments, and maintains study budget
Tracks and reports all adverse events, protocol deviations, and any other unusual activity experienced by assigned investigator sites and communicates with assigned sites on routine matters
Reviews all adverse events reported in clinical study for the identification and evaluation of safety issues and any patterns that are identifiable
Reports safety findings in a summary format to the CTM
Prepares documentation for and attends Clinical Event Committee (CEC) meetings, if applicable
Identifies and documents data errors or items requiring clarification on all documents collected for study and initiates data clarification/validation process after researching source documents
Assists in preparing clinical reports of assigned projects for submission to regulatory authorities
Bachelor’s Degree in life sciences of B.S.N. Nursing degree
Experience in Phase I-IV clinical studies as a clinical trial assistant or clinical research associate is highly desirable
Excellent Communication and writing skills, professionalism and ability to effectively interact with staff and management alike; ability to verbally communicate effectively with management, department clinical research and other team members

248

Clinical Research Associate Resume Examples & Samples

Experience as a clinical research associate minimum of three years
At least 2 years related experience in (conducting) clinical trials (healthcare setting, CRO, medical device and/or pharmaceutical company and/or industry)
40% Travel

249

Senior Clinical Research Associate Resume Examples & Samples

Assess visit type, assess protocol specific and UBC SOP knowledge and assess individual’s ability to perform visit type independently
Mentor team member by sharing tips/tricks/tools reviewing process prior to and after visit
Assists management team by mentoring other CRAs
Assists with preparation and/or delivery of presentations for UBC Academy, departmental training and/or sponsor specific training
Ability to perform tasks in CTMS, EDC, Outlook and client specific systems (if applicable)
UBC-CE1

250

Clinical Research Associate Resume Examples & Samples

Consistently completes site monitoring reports, confirmation/follow-up letters per UBC and/or client SOPs; signs, scans and/or provides to Clinical Site Specialist/Regulatory
Document Specialist for filing in Trial Master File according to UBC and/or sponsor timelines requiring minimal corrections
Ensures follow-up of site issues and action items per UBC/sponsor timelines
Consistently completes SOP review and documentation within requested timelines
Consistently completes sponsor specific training and documentation within requested timeline
Assists PM and management team by being an Assess Instruct and Mentor leader
Minimum of > 24 months active monitoring
Ability to perform tasks in UBC’s Clinical Trial Management System, Electronic Data Capture System, Outlook and client specific systems (if applicable)
Up to 80% travel
LI-CE1

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Lead Clinical Research Associate Resume Examples & Samples

Senior Clinical Research Associate Resume Examples & Samples

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Clinical Research Associate Resume Examples & Samples

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Senior Clinical Research Associate Resume Examples & Samples

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Senior Clinical Research Associate Resume Examples & Samples

Clinical Research Associate Resume Examples & Samples

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