Clinical Mgr Resume Samples

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A Lehner

Abel

Lehner

1108 Leanne Mission

Philadelphia

+1 (555) 907 3646

1108 Leanne Mission

Philadelphia

Phone

p +1 (555) 907 3646

Experience Experience

Boston, MA

Asst Clinical Mgr

Boston, MA

Jacobson-Stokes

Boston, MA

Asst Clinical Mgr

Collaborates with the clinical manager to manage patient care delivery in an effort optimize patient outcomes, customer satisfaction, and resource management
Collaborates with the clinical manager, medical director, and others in developing the strategic plan, direction for the unit, and utilizes CQI techniques
Communicate effectively and work cohesively with a diverse work group
Provides the staff RN with an avenue for formal leadership and professional development opportunities
Implementing tactics to improve performance on the unit
Provides a critical link between staff, leaders and providers
Promote and support an environment conducive to staff growth, development and autonomy

Los Angeles, CA

Proj Mgr, Clinical Outcomes

Los Angeles, CA

Rutherford LLC

Los Angeles, CA

Proj Mgr, Clinical Outcomes

Ensures all necessary study specific training is provided to study team to improve performance and knowledge. Provides coaching / mentoring as necessary
Develops and monitors endpoint adjudication processing workflows to maintain efficiency
Provides feedback to senior management on project status, metrics, client satisfaction and staffing issues.
Facilitates the development of project reports. Generates and distributes project reports to the study team
Performs project finance reporting activities
Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance
Performs user acceptance testing of electronic endpoint adjudication system

present

Phoenix, AZ

Clinical Rsch Prog. / Proj Mgr

Phoenix, AZ

Deckow LLC

present

Phoenix, AZ

Clinical Rsch Prog. / Proj Mgr

present

Provides support and meets regularly with the Principal Investigator concerning HD Program management issues and activities and the status of projects. Identifies and evaluates methods for improving workflow and cost effectiveness and makes recommendations for improvement
Act as a resource for DACCPM regarding federal, state, local laws and regulations governing human-subject research
Keep current on federal, state, local laws and regulations governing human-subject research through attendance at conferences, workshops, seminars, or lectures pertaining to human-subject protection
Instructs and oversees new employee training
Provide guidance to study teams on the process for collecting, reviewing and approving site regulatory documentation
Establishes standards for the delivery of research procedures; acts as a role model by providing excellent service to internal and external contacts
Assist with the program’s grant management, including grant writing and budget preparation

Education Education

Bachelor’s Degree in Health

Florida Atlantic University

Bachelor’s Degree in Health

Skills Skills

Excellent written and verbal communication skillsKnowledge of current and developing clinical research trends
Excellent attention to detail
Ability to effectively supervise and train staff
Strong organizational and , communication skills
Excellent analytical and problem solving skills
Establishes standards for the delivery of research procedures; acts as a role model by providing excellent service to internal and external contacts
Self motivated and able to work well independently
Ability to supervise others and display initiative
Intermediate knowledge of cancer terminology
Strong computer skills and experience working in Google Apps, Microsoft Excel, Word, PowerPoint, Databases, Adobe, and videoconference platforms

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Clinical App & Analytical Svcs Mgr Resume Examples & Samples

BA/BS/BSc in the sciences or RN
5 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical product development (clinical research or clinical operations experience obtained at a biotech, pharmaceutical or CRO company)
Strong understanding of the concepts of clinical research and drug development
Strong understanding and experience in the use of performance management techniques, measurement and visualization
Strong understanding of principals of customer service as it applies to internal and external customers
Advanced computer and system operation skills
Continuous improvement principles and their application e.g., Six Sigma Understanding of project management software
Familiar with other Data Management systems (IVR, EDC, etc.)

Mgr Clinical Trial Info Disclosure Resume Examples & Samples

Degree (Bachelor, State Examination, Diploma) in pharmacy, biology, chemistry, medicine, or equivalent; Master or PhD preferred
About 4-6 years’ experience in the pharmaceutical industry, experience in the area of clinical trial information disclosure highly desirable
Working knowledge of key global laws, regulations and guidelines relating to clinical trial data disclosure is desirable
Good general knowledge of key global pharmaceutical legislation
Experience of working in a global, international regulatory environment and experience in interacting with regulatory authorities. Experience working within a global team framework and a multi‐cultural environment
Excellent research skills. Understanding of drug development and regulatory processes
Experience of interactions with FDA, EMA and/ or EU National Agencies and EMA as well as with industry associations is desirable
Ability to provide technical input, proven ability to plan, coordinate and lead activities simultaneously on multiple projects

Clinical Data Mgmt Mgr Resume Examples & Samples

Development
Relevant Bachelor’s degree
Solid experience in/knowledge of data management in a pharma/biotech/CRO arena
Demonstrated experience working effectively in cross-functional teams
Experience in oversight of outside vendors including Functional Service Provider (CRO’s, central labs, imaging vendors, etc.)
Strong communication, negotiation and leadership skills
Solution orientated, driven to achieve results both decisively and efficiently

Senior Mgr, LTC Clinical Programs Resume Examples & Samples

Conducts quality reviews and initial assessment reviews to ensure personalized plans of care are being developed according to approved medical necessity criteria and WellCare designated criteria along with current clinical knowledge
Ensures that all prospective members are eligible for participation in the Medicare/Medicaid program and that existing members remain eligible
Refers prospective members, who do not have Medicaid, to the Medicaid Applications team
Conducts periodic home visit(s) with Clinical Enrollment staff to monitor their knowledge of Program eligibility criteria and benefits and design
Develops tools to monitor staff productivity and efficiency/efficacy of department policies and procedures
Identifies opportunities for staff development, e.g., sales training, specific disease management protocols
Manages MLTC Enrollment Staff
Responsible for conducting new hire orientation and training
Responsible for ensuring withdrawals and disenrollment's are appropriate and timely
Responsible for organizing and overseeing monthly enrollment staff meeting
Responsible for vendor audits for non-par LHCSA's, ADHC's and SDC's
Liaison for HRA MLTC plan to plan transfers
Liaison to HRA for enrollment problems and capitation issues with new members

Proj Mgr, Clinical Outcomes Resume Examples & Samples

Travel (approximately 35%) domestic and/or international
Manages project in a timely manner in adherence with ICON’s SOP’s, ICH, GCP and appropriate regulation and liaise with other departments as necessary
Delivers projects in accordance with the contract, timelines and study budget*
Identifies out of scope activities and initiates budget change orders and contract amendments
Attends and presents at Investigator Meetings, Client Kick-Off Meetings, and other client meetings*
Facilitates the electronic endpoint adjudication system for the project
Ensures all necessary study specific training is provided to study team to improve performance and knowledge. Provides coaching / mentoring as necessary
Develops and maintains all trial documentation (ie Charter, Procedure Manual, Site Manual, Adjudication Forms, Communication Plan, System Requirement Specifications, Data Transfer Specifications, and Committee Training Manual)
Performs user acceptance testing of electronic endpoint adjudication system
Performs data reconciliation*
Serves as the primary study contact for client and internal and external study teams
Leads internal and external study team meetings
Leads internal endpoint adjudication processing team
Develops and monitors endpoint adjudication processing workflows to maintain efficiency
Prepares meeting agenda and facilitates the completion and distribution of meeting minutes
Facilitates the development of project reports. Generates and distributes project reports to the study team
Coordinates Endpoint Adjudication Committee members and adjudication process
Conducts project/system specific training to committee members
Implements Quality Control measures for adjudication process and adjudication outcomes as necessary
Performs project finance reporting activities
Provides feedback to senior management on project status, metrics, client satisfaction and staffing issues.*
Participates in bid defense and new proposal review activities as necessary
Participates in internal, client, and regulatory audits*
US/LATAM/CAN: Prior clinical trial experience
EU/APAC
Basic knowledge of applicable global, regional, local clinical research regulatory requirements; ie Good Clinical Practice (GCP) and International Conference of Harmonization (ICH) guidelines, standard operating procedures (SOPs), or the ability and willingness to gain this knowledge
Ability to interact effectively and professionally with various levels of staff for both internal and external departments, vendors, or Sponsors
Excellent computer skills (Microsoft Word, Excel, PowerPoint, Outlook). Experience working with electronic data capture and transfer methods
Excellent communication and documentation skills
Excellent organizational, time management and problem-solving skills
Strong sense of responsibility and dedication
Attentiveness to detail and accuracy; ability to maintain quality standards
Ability to follow instructions/guidelines, utilize initiative and work independently
Proven ability to multi-task, manage competing priorities and timelines
Ability to manage team members and processes
Willingness and aptitude to learn new skills

Clinical Prog Development Mgr Resume Examples & Samples

Oversees the creation and implementation for programs relevant to the organization's strategic initiatives involving Health Services clinical, administrative, and operational input
Acts as the content and technical subject matter expert to the operation managers and directors for key project initiatives including the development of detail work plans, setting deadlines, assigning responsibilities, and monitoring/summarizing project progress
Prepares strategic analysis of potential business and/or operational opportunities in relation to new business, transition of care, and MEI targets using customized solutions
Preferred A Master's Degree in a related field Business or HC Management (MBA, MHA, MPH, MSN)
Preferred 2+ years of experience in managed care, plus utilization management, care coordination, disease management, medicare, medicaid, DSNP, dual eligibles, PCMH
Advanced Ability to implement process improvements
Required Advanced Microsoft Outlook
Required Advanced Microsoft Visio
Required Intermediate Other Ability to interpret an extensive variety of technical instructions in mathematical form and deal with several abstract and concrete variables

Clinical Data Mgr Resume Examples & Samples

Data management leadership on a large I global project, or multiple projects with responsibility for the development of the project Data Management Plan; data management systems set-up; and data accession, data entry and data review specifications and processes; and oversight of data management activities for the delivery of clinical data according to client quality and integrity specifications, and project timelines and budgets
Financial management of gross revenues in excess of $250K per year
In depth knowledge of clinical trial process and data management, clinical operations,
Working knowledge of the relationship and regulatory obligation of the CRO industry with

Asst Clinical Mgr Resume Examples & Samples

Assessments - Collects, prioritizes, and synthesizes comprehensive data pertinent to the patient’s health or situation
Diagnosis - Analyzes assessment data to determine nursing diagnoses
Outcomes Identifications - Identifies expected outcomes individualized to the patient
Planning - Develops a plan that prescribes interventions to attain expected outcomes
Implementation - Implements the identified plan
Evaluation - Evaluates the patient’s progress towards attainment of the outcome
Quality of Practice - Systematically enhances the quality and effectiveness of nursing practice
Education - Attains knowledge and competency that reflects current nursing practice
Professional Practice Evaluation - Evaluates one’s own nursing practice in relation to professional practice standards and regulatory guidelines
Collegiality - Contributes to the professional development of peers, colleagues, and others
Collaboration - Collaborates with patient, family, and others in the conduct of nursing practice
Ethics - Acts in an ethical manner
Research - Integrates research findings in practice
Resource Utilization - Incorporates factors related to safety, effectiveness, cost, and impact on practice in planning and delivering patient care
Leadership - Provides leadership in the professional practice setting and the profession
Being involved in house-wide committee of assigned quality metrics
Bringing education to the staff at the unit level
Implementing tactics to improve performance on the unit
Being aware of the current metrics and ensure performance and measurement to goal is communicated to staff

Mgr Regional Clinical Resume Examples & Samples

Manage clinic nursing services and supervise clinical team leaders from each site
Responsible for oversight of clinical process and clinical process improvement by analyzing and reviewing nursing processes to increase efficiency
Responsible for ensuring the technical skills of nursing personnel are in accordance with office policy at their site
Responsible for maintaining properly operating medical equipment and Instruments
Responsible for orientation content for new nurses and provides support on an on-going basis
Development of clinical nursing goals and objectives
Recommend and implement nursing policies and procedures, and participates in performance evaluations for all clinical staff in the organization
Responsible for oversight and management of clinical licenses and certifications
Responsible for coordination with the Practice Administrators for performance issues, process improvement, and progressive discipline
Maintain knowledge of trends and developments in the field by reading appropriate articles, journals and related material
Participate in monthly facility meetings to facilitate improvement of clinical quality targets or other clinical processes as assigned, meeting and maintaining the requirements of NCQA standards for Medical Home
In collaboration with the Managing Directors and Practice Administrators, identify opportunities to standardize best practices across clinics
Perform any other job-related duties as assigned by the VP of Clinical Services
Conducts routine on-site assessments for clinics in designated regions
Obtains and analyzes data to assist in workload planning to meet the needs of each clinic
Supervises clinical team leads and ensures that nursing care provided to patients is effective in delivery and follows established standards of practice
Interacts with VP of Clinical Services, managing Directors, Practice Administrators, and/or Human Resources in resolving complex employee relations problems of the clinical staff

Assoc Mgr Clinical Mgmt-shanghai Resume Examples & Samples

Conducts regular performance appraisals and career discussions with staff
Facilitates employee career development. Interviews, recruits and selects staff
Manages and conducts induction/orientation programs for all new employees, ensuring their smooth assimilation into the company
Ensures all staff CVs, training records, position profiles and experience profiles are complete and up-to-date
Delivers training on Working Practice Documents (WPDs) and Standard
Identifies training gaps and ensures that training requirements are met. May contribute to development of training programs, where appropriate
Demonstrated effective mentoring/leadership/supervisory ability
Excellent clinical trials monitoring skills; Remote and on-site
Excellent team player with team building skills

Mgr Adv Clinical Applications Resume Examples & Samples

Collect EHR deficiency data related to Advanced Clinicals and future Meditech projects
Managing unsigned orders and provider documentation
Managing incorrectly signed and rejected orders
Manages correction and completion of PDoc entries
Collaborates with providers and HIM to define workflow processes that promote electronic authentication of electronic orders
Establishing and maintaining the data integrity auditing process
Serving as a liaison between HIM and the DAC
Ongoing support to the DAC to assist in the reduction of telephone and verbal orders
Provides oversight, guidance, and ongoing support to the development and sustainability of a new CJW Nursing Informatics Council
Assists in identifying gaps/areas of opportunity for improvement in clinical documentation and in the creation of action plans for improvement
Guides Nursing Informatics Council to seek technology driven processes to increase efficiency in workflow, patient safety, high quality care and reduce costs
Actively supports and promotes systems standardization, utilization, and best practices in the areas of CPOE initiatives
Assists in finding resolutions to issues related to CPOE initiatives, including processes and workflows. Escalates appropriate issues to the DAC
Actively participates on the Advanced Clinicals Committee
Assists in the conversion and upload of all EBOS to downtime share point site
Assists in the execution of Meaningful Use objectives and documentation of meeting Meaningful Use criteria
Other duties as assigned by the director
Minimum requirement of Associate’s Degree from an accredited school of Nursing. Bachelor’s degree preferred
Possess working knowledge of Microsoft: Word, Excel, Outlook, Access, PowerPoint
Knowledgeable in Meditech charting and reporting systems – to include new CPOE platforms and changes
Develop and present educational material to various audiences
Demonstrates effective communication and organizational skills
Ability to handle stressful environment and multiple projects simultaneously
Previous managerial experience and or IT&S/Nursing Informatics Experience
Hospital Experience Preferred

Mgr, Clinical Technology Resume Examples & Samples

Manages planning, coordination and expense priorities for overall clinical technology service area budget. Ensures purchases are coordinated with service area local Clinical Technology review/approval process and structure including validation of area purchases that purchased equipment meets demand and efficiency metrics
Accountable for successful operations and meeting Service Level Agreements (SLA). Manages Clinical Technology staff and resources for service area(s). Evaluates/assesses and allocates appropriate resources to meet demands (i.e. people and dollars)
Minimum five (5) years of experience in leadership/supervisory role
Professional certification as a Certified Clinical Engineer and/or certification in Biomedical instrumentation (CBET, CLES, CRES), or Computer certification CompTIA A+ preferred
Master's degree in related field (i.e. health administration, MS engineering, and MBA) OR six (6) years of experience in a directly related field

Mgr, Clinical Ops Oversight Resume Examples & Samples

Manages and develops direct reports who include supervisory and/or exempt professional personnel including but not limited to hiring, mid-year and annual reviews, Performance Improvement Plans (PIP), terminations, etc
Develops and implements case management workflows and policies & procedures
Collaborates with other departments cross functionally regarding case management and/or Clinical Services initiatives
Partners with Management team to develop audit plans that identifies and prioritizes areas of significant risk
Reviews and audits the effectiveness of corrective action plans that address report findings and provides comprehensive follow-up to senior management at least monthly
Develops, implements and manages process improvement initiatives
Manages audit planning, including review of audit programs for multiple performance reviews specific to role or department
Evaluates performance of audit staff and provides timely verbal and written feedback
Applies a comprehensive knowledge of Care Model for telephonic and field care management programs
Proactively monitors appropriate metrics to improve both quality and drive efficiency
Partners with key stakeholders across clinical and non-clinical departments during external and internal audits in order to provide appropriate documentation and communication to ensure the audits are conducted in accordance with audit methodology, professional standards, NCQA, CMS, and state Medicaid requirements
Develops QA standards to monitor and improve adherence to department standards, policies and procedures, templates, formats and guidelines
Develops and implements studies of business function systems to include performance audit scores, action plans, and analysis. Prepares narratives and graphic display of the findings
Direct involvement in building collaborative relationships with other departments to resolve quality issues and barriers, i.e Provider Network, Quality, Advocacy, Utilization Management, etc
Required A Bachelor's Degree in Nursing, Health Administration, Business Management or related field
Required or equivalent work experience 5+ years in nursing, a clinical setting, managed care, or business reporting/analytics
Required 5+ years of experience in practical work in a business environment with data collection, creation and analytics
Required 2+ years of experience in leading/supervising others
Preferred 2+ years of experience in an acute clinical care setting and/or managed care related experience
Preferred 2+ years of experience in Case management
Advanced Ability to identify basic problems and procedural irregularities, collect data, establish facts, and draw valid conclusions
Advanced Demonstrated analytical skills
Advanced Knowledge of healthcare delivery
Advanced Other Knowledge of NCQA, CMS, and state Medicaid requirements
Advanced Ability to effectively present information and respond to questions from peers and management
Intermediate Ability to work independently Ability to work independently, handle multiple assignments and prioritize workload
Intermediate Ability to drive multiple projects
Intermediate Ability to create, review and interpret treatment plans Ability to create, review and interpret treatment plans
Intermediate Demonstrated negotiation skills
Intermediate Ability to lead/manage others Intermediate Ability to implement process improvements
Required Advanced Other reporting analytic software (i.e. Tableau)
Preferred Intermediate Microsoft Visio

Regional Clinical Trial Mgr Resume Examples & Samples

Providing regional input into operational planning activities
Management and reporting of clinical studies in region conducted by Global Development through oversight of study activities, identification and resolution of issues, and communication of study timelines/deliverables to GCTM
Ensuring implementation of study(ies) in accordance with SOPs and ICH/GCP guidelines
Management of study budget and timelines
Management of vendors to the required standards (may include vendor set up and oversight through the course of the study)
Bachelor’s degree ( or higher qualification) & 5 years of directly related experience
Experience in oversight of external vendors (e.g. CROs, central labs, imaging vendors, etc.)
Advanced knowledge of clinical trial management including regulations and guidelines across multiple countries
Extensive knowledge of ICH/GCP regulations and guidelines
Project and Program management including oversight of study deliverable, budgets and timelines
Key performance indicators (KPIs)

Clinical Data Mgmt Mgr Resume Examples & Samples

Training and mentoring of DM TA staff on processes, projects and programs
Lead or participate in the development, review and implementation of processes, policies, SOPs and associated documents affecting DM
Participate in and/or lead DM and cross functional working groups
Contribute to the continuous improvement of DM and the wider Development organization through information sharing, training and education
Contribute to development of DM outsourcing strategies and long-term relationships with CRO partners / external vendors
Promote and be an advocate of DM internally and externally
Represent DM at project team meetings i.e., GCST
Project level coordination of and day to day oversight of DM tasks including
Co-ordination of lead DM’s within the project
Review of all DM documents within a project area to ensure a consistent approach
Overview of project timelines and metrics to ensure databases are delivered to set timelines
Approve database locks and unlocks
Ensure that quality control checks are occurring such that quality databases are delivered
Develop and co-ordinate project level training for data management staff
Review and approve study specific training
Manage vendor deliverables and relationship at the project level
Communication and escalation of project level issues including processes, timelines, resourcing, performance, etc
Review of all study level non DM documents for awareness and project level consistency
Lead electronic submission activities
Assist with response to questions and findings from Clinical Quality Assurance (Quality Assurance) and other audits at the study / vendor level

Asst Clinical Mgr Resume Examples & Samples

Provides coordination of all nursing care from the point of admission through discharge
Works in collaboration with multi-disciplinary team members, appropriately delegates nursing care to other direct care team members
Facilitates smooth operations among the multi-disciplinary team through networking and relationship building
Accountability in the areas of staff and patient education, performance evaluation, day-to-day operations and supporting the change process
Provides a critical link between staff, leaders and providers

Clinical Trial Mgr, Tm Resume Examples & Samples

Reviews site qualification criteria and manages the identification process of potential investigators and clinical sites; oversees, participates in pre-study site visits, reviews evaluative reports; makes final selection of study sites
Reviews CTAs in conjunction with relevant internal departments (as necessary)
Obtains essential documents required for approving shipment to investigational site
Tracks and assesses study budgets as they relate to actual study progress, timelines, and/or work being performed by outside vendors (CROs, CRAs, centralized laboratories, etc)
Manages Investigator Meetings
Continuously evaluates quality of site monitoring and associated documentation
Coordinates vendor activities as necessary
Ensures adequate Serious Adverse Event reporting documentation, tracking and follow-up
Responsible for maintaining Trial Master File
EDUCATION: Bachelor's Degree

Clinical Rsch Prog. / Proj Mgr Resume Examples & Samples

Provides support and meets regularly with the Principal Investigator concerning HD Program management issues and activities and the status of projects. Identifies and evaluates methods for improving workflow and cost effectiveness and makes recommendations for improvement
Interprets and applies GCP and IRB policies to support research compliance
Provides both administrative supervision and support to clinical research coordinators and MRI technicians
Instructs and oversees new employee training
Oversees and monitors employee work schedules, timeliness, and productivity. Tracks project performance
Establishes standards for the delivery of research procedures; acts as a role model by providing excellent service to internal and external contacts
Establishes expectations for teamwork and collaboration and actively coaches employees to meet those expectations
Establishes relationships and acts as a liaison to other departments within the research center
Develops, implements, and oversees the maintenance of filing and record keeping, of research materials
Evaluates and standardizes operating procedures (SOPs) and effectively troubleshoots and resolves issues
Oversees all purchasing for the program and research studies. Assesses equipment acquisition and training needs and makes recommendations to the Principal Investigator. Orders equipment and supplies for the program
Fosters a process of continual improvement in execution of research procedures
Establishes and monitors quality performance metrics
Ensures that program processes protect the privacy and security of confidential information
Assists in the preparation for Clinical Trial Monitoring visits and internal/external reviews
Performs other duties as assigned by the Principal Investigator
May be involved in the direct conduct of clinical trials
Advanced time management and analytical skills
Ability to organize information
Ability to handle sensitive information with absolute confidentiality
Working knowledge of software applications including Microsoft Word, Excel and Power Point
Ability to make effective decisions independently and/or to escalate issues as needed
Ability to multitask in a challenging environment
Ability to effective train and supervise the work of others

Clinical Rsch Prog. / Proj Mgr Resume Examples & Samples

Coordination, monitoring and timeline management of multiple clinical trials and research projects within the program
Ongoing monitoring and evaluation, across all participating sites, of protocol, regulatory and data compliance and assessment of compliance with federal and local regulations
Working directly with entities within and outside the organization, including PIs, Sponsors and collaborators, to resolve workflow issues and improve process
Identifying changes associated with Standard Operating Procedures and developing processes to ensure compliance
Ensuring timely reporting to all sponsors, monitoring, safety and regulatory boards (e.g. FDA, IRB, DSMB, etc)
Training of new staff and assessment of ongoing continuing education needs
First-line supervision of research staff, especially on coordination of their own research portfolio
Assisting staff with task prioritization for project assignments
Mentoring junior staff
Executing new hire, corrective action and performance evaluation processes for direct report research staff
Staying current with federal and local regulations, guidance and quality assurance trends as they pertain to the conduct of clinical research
3-5 years related experience
Exceptional project management, time management and organization skills
Excellent written and verbal communication skillsKnowledge of current and developing clinical research trends
Sound interpersonal skills and the ability to supervise others
Ability to work independently and display initiative
Demonstrated ability to successfully manage multiple projects and tasks
Established rapport with investigators and sponsors with the ability to resolve operational matters
Ability to effectively supervise and train staff
Familiarity with the Code of Federal Regulation (CFR) and Good Clinical Practice (ICH GCP)
Occasional domestic travel required

Clinical Territory Mgr Inf-wausau Resume Examples & Samples

Develop and execute strategic plans to grow infusion business in key accounts
Meet a defined market infusion revenue budget by servicing and growing existing business
Assist the market manager in growing infusion therapy business through accurate business projections, goals, specific strategies and pertinent account information
Work closely with clinical branch personnel to ensure the highest level of customer satisfaction with the goal of delivering the best service possible to patients receiving these critical therapies in the comfort of their homes

Asst Clinical Mgr Resume Examples & Samples

Communicate effectively and work cohesively with a diverse work group
Work collaboratively with internal/external customers
Demonstrated a commitment to patient focused care
Demonstrated ability to prioritize independently and respond to multiple simultaneous requests
Demonstrated ability work in a fast paced environment with established time constraints and in difficult situations
Serves as a role model for RN professional practice
Collaborates with the clinical manager to manage patient care delivery in an effort optimize patient outcomes, customer satisfaction, and resource management
Promote and support an environment conducive to staff growth, development and autonomy
Current IL RN graduate from accredited school of nursing with BSN preferred
Charge RN with 1 year experience or
5 years of nursing clinical experience with Med-Surg background preferred
Demonstrated leadership experience preferred
Certification in specialty areas, if applicable within 1 year of hire

Mgr Clinical & Rev Cycle Apps Resume Examples & Samples

Candidates must have a minimum of 3 years’ experience managing implementations of large-scale, complex, multi-disciplined, cross-functional and highly visible projects/programs and cross organizational teams
Significant project management experience with proven ability to manage, execute, control and achieve closure of large, complex projects is required
Experience with business process redesign, benefits realization and project planning in a healthcare environment
Possess a strong background in healthcare with large software application design and implementation projects
Demonstrate the ability to work collaboratively with clinical departments and cross-functional teams, and to deliver projects on time and on budget
Significant experience in evaluating software packages and working with application vendors and system integrators
Excellent Project Management skills including practical usage of Microsoft Office Products. Must possess strong communication, presentation and customer relation skills
Experience managing large complex projects and has strong project management skills
Demonstrates extensive experience in client relationship management
Must be deeply experienced in Project Management Methodologies
Excellent analytical ability and interpersonal skills to communicate effectively with clients and other IT staff
Demonstrated effectiveness interfacing and negotiating with clients, internal customers and vendors
Leadership and ability to motivate others

Clinical Implement Proj MGR Resume Examples & Samples

Maintains standardized corporate templates of materials utilized in implementations including those corporate materials reviewed and approved by CMMC
Collaborates with the management team in the corrective action process by gathering documentation regarding noncompliance in meeting required standards. Contributes to performance improvement plans and participates in discussions regarding individual performance and system issues
Ensure processes are in place to support compliance with all state and federal laws (HIPAA), regulatory requirements, accrediting agencies (NCQA and URAC) as well as Beacon clinical criteria and policies and procedures
Identifies improvements or training opportunities and develops/presents quality improvement training materials to improve overall service quality. Identifies trends and concerns in system use and workflows and applies corrective actions as necessary to meet business needs
Collaborates with the management team on new client implementation activities, including development/presentation of training materials, to ensure all home service center and client performance expectations are met. Assists service center clinical implementations staff in training of new staff working with system trainers. Develops and provides clinical trainings as necessary
Using approved documentation performs testing of core and non-core system enhancements to assure product performs in a satisfactory manner. Maintains a log or record of problems encountered during testing. Assists in validation of migrated and converted data in support of Model Office procedures. Participates in post-production testing at various releases during year
Designs and develops test scenarios and scripts to validate software product meets requirements of the approved functional and technical specifications and does not interfere with existing service center specific workflows. If issue is identified works with service center management and national operations to correct issue in application or modify workflow to accommodate system change
Assists in the researching of errors identified in Level III testing
Coordinates with corporate trainers in the training of personnel in correct procedures for data entry and updates of clinical information with new enhancements in the Clinical Connect application while utilizing release notes and other materials provided by National IT Trainers during the Train the Trainer Sessions with releases
Assists in researching and answering questions from users regarding new system functionalities and enhancements
Assists in researching reported production system errors within the service center
Microsoft Office (Word, Excel, Access, Outlook, Powerpoint, Project and Visio) skills
Experience with Clinical Systems
Analytical and problem solving ability
Group presentation and public speaking skills
Collaboration and team-oriented work philosophy

Assoc Mgr Clinical Mgmt-australia Resume Examples & Samples

Manages staff, providing coaching, mentorship and work direction
Ensures timeliness and accuracy of timesheets and expense reports
Supports allocation activities per the local resourcing process
Supports activities of project managers and clinical team managers to optimize the operational running of projects. Escalates appropriately any issues which may impact project deliverables
Operating Procedures (SOPs), local requirements and any other subjects that impact clinical operations
Alerts management to quality issues, requests QA audits as appropriate, and facilitates client and internal quality assurance audits as required
Ability to evaluate medical research data

Clinical Mgr Resume Examples & Samples

B.S.N. required; a Master's degree in Nursing or in a health-related field is preferred (may be in progress)
Three (3) years clinical leadership experience and ability to demonstrate competency in management skills
At least (3) years clinical nursing experience is required; and at least one year of related nursing experience required
Ability to organize, prioritize and delegate appropriately

Asst Clinical Mgr / Csdu p Resume Examples & Samples

3 years of nursing specialty experience
Associate Degree of Nursing or Bachelors of Science in Nursing (preferred) from accredited school of nursing - 2 years of nursing exp. if ADN
Non BSN nurses must start a BSN program within two years of hire date and complete within 5 years (tuition assistance available)
Current Illinois RN license
Ability to respond quickly to patient needs and work at fast pace
Adequate time management and organizational skills
Familiarity with patient care equipment
Ability to work weekends, holidays, and different shifts in order to accommodate staffing
Certain positions may need to take call

Asst Clinical Mgr ICU Resume Examples & Samples

Performance of the principle duties and responsibilities of the RN position and serves as a role model for professional practice
In collaboration with the clinical manager, manages patient care delivery to optimize patient outcomes, customer satisfaction, and resource management
Promotion and support of an environment that is conducive to staff growth and development and autonomy
Responsibility for professional growth and development

Clinical Rsch Prog. / Proj Mgr Resume Examples & Samples

Work closely with the Principal Investigator to implement a quality control system related to all activities of the clinical and regulatory program
Map, organize and implement a documentation system for each device development project in the Tearney laboratory. Writes operations manuals. Edits manuscripts
For each device developed in the Tearney lab, prepare a design development plan document that includes device control, device fabrication and clinical usage. Assume overall responsibility for the preparation of documentation templates and document control
Ensure that all aspects of adherence to all rules and regulations set by the institution, the granting agencies and the FDA are complied with at all times through provision of on-going SOP development and training
Oversee maintenance of QC/QA documentation efforts
Prepare related reports and work with PI on oversight of QA program compliance
Must be able to function independently and make effective decisions
Must demonstrate excellent judgment and aptitude in problem solving
Must have strong organizational, administrative and time management skills
Must have excellent oral and written communication skills as well as interpersonal skills, with ability to interact professionally at all levels
Ability to work both independently and as part of a team is essential
Must have strong database management and computer skills

Mgr, Clinical Protocol Admin Resume Examples & Samples

Clinical Care Standards
Coordinates systems to improve quality of care, manage utilization of resources and improve effectiveness of services
Provides appropriate supervision of staff responsible for standard and research sample acquisition and processing
Clinical Research and Logistics
Liaison with Principal Investigators and study sponsors to develop clinical studies design
Directs all regulatory requirements (internal and external)
Assesses resource needs by devising budgetary and programmatic requirements for all new research projects
Provides statistical expertise in the design and analysis of clinical and laboratory clinical research projects
Responsible for instruction of faculty and staff in clinical research analysis
Program Informatics
Manage research information systems for all program functions including but not limited to implementation of system modifications, upgrades and broad-based data management systems
Manage, design and implement new reporting tools and changes to reporting systems including statistical reporting. Ensure that appropriate instruction to faculty and staff is properly carried out
Direct all data management activities for the AML, MDS, and CML Programs. Responsible for general supervision of all program staff
Identify, develop, propose and implement new mechanisms for improving or enhancing program operations
Research Grant Programs
Develop new grant initiatives including proposal development and submission as well as implementation of the funded program
Responsible for reporting to the medical director/section chief, initiate grant non-competing renewals and progress reports
Advise faculty on the potential for program funding, and new areas of development
Philanthropy/Development Programs
Represent the program medical director to current and prospective donor program representatives
Responsible for proposal development and presentation, and the negotiation of new projects
Program Finance
Research financial issues related to clinical research, patient care service

Asst Clinical Mgr-post Surg Resume Examples & Samples

Practices professional nursing to provide patient care through the use of the nursing process of assessment, diagnosis, outcome identification, planning, implementation and evaluation
Provides the staff RN with an avenue for formal leadership and professional development opportunities
Brings a clinical perspective to decisions and can provide sound input that reflects the needs and strengths of the unit
The role supports the infrastructure and leadership necessary to ensure this professional and paraprofessionals do their work in an environment that supports their success resulting in organizational solvency

Senior Mgr, Clinical Outsourcing Resume Examples & Samples

BA/BS in scientific or business discipline required
Direct experience (5 yr. minimum) in managing clinical contracts within the pharmaceutical industry within a clinical procurement/outsourcing function to include experience in the negotiation of contracts with Phase I-IV CROs, technical service providers, consultants etc
Demonstrates business/financial acumen and thorough understanding of CRO cost models and budget as well as services and costs associated with functional service providers (e.g. IVR, Central Labs, Biostatistics, and Medical Writing, Imaging, ECG, ePRO)
Clear understanding of the drug development process
Thorough knowledge of GCP/ICH Guideline and Regulations

Clinical Rsch Prog. / Proj Mgr Resume Examples & Samples

Design protocols for international projects and evaluate program progress
Design online questionnaires for healthcare practitioners
Develop data collection tools for our international project sites
Prepare grant applications and budgets
Strong computer skills and experience working in Google Apps, Microsoft Excel, Word, PowerPoint, Databases, Adobe, and videoconference platforms
Intermediate knowledge of cancer terminology
Ability to supervise others and display initiative
High level of time management and organization skills
Strong organizational and , communication skills
Self motivated and able to work well independently
Able to collaborate with a varied group of researchers and clinicians, including physicians, nurses, social workers, and clinical research assistants, both domestically and globally
Must possess strong budget management skills
Ability to make independent effective decisions
Minimum of 5 years of experience required
Prior Supervisory experience strongly preferred

Mgr Clinical Dietitians Resume Examples & Samples

Maintains and develops client relationships and client satisfaction for nutrition care of patients and residents
Plans projects, including defining objectives, scope, specifications, methods, timetables, staffing and budget
Manages all activities and communication from the diet office
Accountable for the execution of service quality by maintaining highest level of delivery
Promotes and supports workplace diversity initiatives
Minimum of 2-4 years clinical experience in an acute care facility, prefer completion of traineeship/fellowship in neonatal nutrition or related clinical experience in neonatal nutrition

Mgr Clinical Mcicu Resume Examples & Samples

Bachelor's Degree in Nursing (BSN) OR Bachelors Degree any field with a Master's Degree in Nursing (MSN)
5 years of relevant clinical experience
Demonstrated leadership experience
8 hours or equivalent education activities of the annual CEUs shall be related to cerebrovascular disease
Effective communication skills in a group setting
Current RN licensure in Illinois
Ability to work within a rapid changing environment
Ability to work collaboratively with internal/external customers
24-hour accountability for patient care issues
Serves as chief retention officer for unit/dept
Manages, develops, implements and evaluates standards of nursing to facilitate quality patient care, efficiency and cost effectiveness
Prepares of departmental budgets (supplies, equipment, personnel). Responsible for budget management and performance and fiscal oversight of all areas of responsibility

Clinical Rsch Prog. / Proj Mgr Resume Examples & Samples

The Clinical Research Regulatory Manager will support all aspects of clinical research including the submission process (IRB/Partners), adherence to Standard Operating Procedures (SOPs,) and procedures and all applicable federal regulations and guidelines of those clinical investigators/investigations that have been selected by the Director for Clinical Research DACCPM, in agreement with the Research Council of the DACCPM
The Clinical Research Regulatory Manager will review related human research protocols and consent forms for completeness and accuracy as well as adherence to all applicable federal/state regulations and institutional policies and guidelines governing protection of human subjects in research
Review consent forms to ensure that they contain all the basic required elements for informed consent, as required by federal regulation, and work directly with the investigators with editing/rewriting for readability at an 8th grade reading level using principles of “plain language.”
Identify requirements for ancillary committee reviews, and other departments, groups, or individuals within each site that share responsibility for human subject protection
Attend meetings of the DACCPM Research Council as needed
Provide guidance to study teams on the process for collecting, reviewing and approving site regulatory documentation
Provide guidance and oversight on maintenance of study Trial Master Files, as appropriate
Keep current on federal, state, local laws and regulations governing human-subject research through attendance at conferences, workshops, seminars, or lectures pertaining to human-subject protection
Act as a resource for DACCPM regarding federal, state, local laws and regulations governing human-subject research
Ensure timely and accurate accrual, enrollment and submissions and approved trials and ensure adherence to study timelines
Train and mentor Clinical Researchers and staff assistants in all above clinical research topics
A master’s degree is required
Minimum of three years experience working in project management related to clinical research, academic research, or similar environment required
Background/familiarity with anesthesia, critical care and pain clinical research as detailed above
A solid understanding of clinical research methodology, FDA, IRB and regulations as well as GCP is required