Research Coordinator Resume Samples

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R Roob

Roel

Roob

915 Rolfson Islands

San Francisco

+1 (555) 381 2062

915 Rolfson Islands

San Francisco

Phone

p +1 (555) 381 2062

Experience Experience

Boston, MA

Research Coordinator

Boston, MA

Wolf, Stiedemann and Becker

Boston, MA

Research Coordinator

Help identify problems with clinical trial start-up and management. Assist with organized improvement efforts and developing research study design improvements
Works with department supervisor/manager to assist and train new hires in the research department/across all specialties
Works directly with faculty to design and improve data collection efforts. Manages all data collection
Work with the Principal Investigator (PI) to develop and update study protocols, including the development of new measures
Assist in background research for the proposed quality improvement projects and support toolkit development for hospitals across IL
Supervises research personnel and ensures orientation and training, performance management, and career development
Assign work; ensure proper workflow of the unit; act as lead worker

Chicago, IL

Senior Research Coordinator

Chicago, IL

Collier-Brown

Chicago, IL

Senior Research Coordinator

Makes recommendations for program enhancements, performance improvement, and "best practices."
Manage qualitative workflows and pipelines from across the network
Supervise the work of employees in supporting roles, including assigning workload and reporting on employee performance
Works collaboratively with manager to monitor metrics
Provides leadership for data management activities
Oversee and manage vendors for execution of online work as well as moderate members of community sites to ensure quality research feedback
Provide general administrative assistance

present

Boston, MA

Senior Clinical Research Coordinator

Boston, MA

Hodkiewicz-Mueller

present

Boston, MA

Senior Clinical Research Coordinator

present

Develops work flow policies and procedures for assigned trials
Develops work flow policies and procedures, prepares manuals and documents related to operations of the function
Develops study budgets and assumes grant management responsibilities
Assist other members by educating, providing resources and consulting on difficult protocols or projects
Provide direct supervision to non-exempt staff (i.e. hiring/firing, performance evaluations, disciplinary actions, approve time off, etc.)
Provide direct supervision to non-exempt staff (i.e. hiring/firing, performance evaluations, disciplinary
Plans, performs, and designs statistical analysis of findings

Education Education

Bachelor’s Degree in Healthcare

Ashford University

Bachelor’s Degree in Healthcare

Skills Skills

Proven ability to produce work quickly and of high quality
Excellent organizational skills and demonstrated ability to complete detailed work accurately
Excellent oral and written communication skills, excellent knowledge of grammar and sentence structure
Comfortable with managing multiple projects simultaneously, with ability to switch focus between projects quickly
Strong work ethic, excellent organization skills, and meticulous attention to detail
Basic knowledge of SQL
Careful attention to detail and an ability to anticipate future problems
Ability to manage and develop new projects whilst maintaining quality across existing ones
5) Demonstrated attention to detail, organizational skills, and excellent written and oral communication skills
Strong computer knowledge and experience with MS Office (Excel, Word, PowerPoint, Access), Outlook, and Photo Shop

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15 Research Coordinator resume templates

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Research Coordinator Resume Examples & Samples

Candidates must thrive in a high-energy environment, be detail oriented and aggressively diligent
Must be a proactive thinker who can handle multiple projects and responsibilities at once
Must have both strong math acumen and analytical thinking and possess good communication skills – both face-to-face and written
Must have strong interpersonal skills and be able to effectively work with a diversity of teams across the organization
Must be well organized and able to meet tight deadlines
Media research knowledge and/or exposure to media research tools a plus
Knowledge of and passion for pop culture and reality television required

Research Coordinator Resume Examples & Samples

Work in conjunction with the Director and VP of Research on the tracking, analyzing and positioning of relevant research information (e.g. TV audience, fan base and attendance data)
Support Director, Research with creation of regularly issued research reports
Provide pertinent research information and analyses to support specific MLB business initiatives
Assist in the design and implementation of proprietary research studies
Help maintain and operate the MLB research fan panel
Maintain a library of media, consumer, and research information

Research Coordinator Resume Examples & Samples

General administrative duties including answering telephones, calendar scheduling, arranging drive-ons, copying and faxing, filing, and planning all travel arrangements
Maintain budgets for the department’s projects and admin needs, including maintaining files, vendor contracts, and research reports
Coordinate meetings and events
Sort and log mail and follow-up where necessary
Communicate information for SVP to executives and coordinators
Manage speaking engagements, publicity events and functions of SVP
Conduct research on request and maintain a general awareness of industry trends, formats, talent and competitive environment
Occasionally assist the data analyst with survey programming, data processing, and building presentation decks
Facilitate the NBC Intern program involvement with department
Cover for other department assistants as needed
Maintain a high level of confidentiality with commitment and dedication to the executive office
Minimum 1 year relevant work experience
Proficiency in Microsoft Office including Excel, Word, PowerPoint, and Outlook
Previous work experience at a studio, network or agency Experience working in a fast-paced environment
Knowledge of TV ratings/analyses and use of Nielsen software such as GALAXY EXPLORER
Some knowledge of SPSS
Detail-oriented and with excellent organizational skills

Market Research Coordinator Resume Examples & Samples

Planning and coordinating activities relevant to customer experience programs such as the collection and analysis of actionable insights linked to research data
Planning, implementation, and maintaining data collection and analysis systems in support of research efforts
Ensures the smooth and efficient operation of research and data collection activities, to identify common loyalty drivers and customer painpoints to assist with driving process improvement initiatives based on actionable insights
Acts as the primary administrative point of contact for Europe for customer experience research efforts
Monitors the progress of specified research activities; develops and maintains records of activities, and prepares reports as required by the business
Prepares and distributes research output in a user-friendly format for effective results interpretation, using appropriate techniques and tools
Interacts with relevant parties to ensure all aspects of specified research programs are executed within the allocated timelines
Ensures effective communication and collaboration with key stakeholders to identify, capture and progress program enhancement requirements, working with reporting line manager to introduce required changes
Gathers datafiles, reports and other associated materials or documentation, filtering same to relevant parties within specified timelines
Is solely responsible for capturing input from external and internal stakeholders, filtering same to reporting line manager prior to addressing same

Research Coordinator Resume Examples & Samples

Organising point to point marketing/company related trips
Ownership of the schedule ensuring optimum efficiency
Monitoring target client lists versus execution
Coordinating with sales people and clients
Organising logistics
Coordinating & distributing presentations & marketing materials
�Gate Keeper� for Client & Distribution Lists for Politics, Banks and Insurance teams
Monitor coverage across tiered accounts and flag/chase down any omissions/gaps
Ensure appropriate correlation between focus/tiered accounts & distribution lists (email//hardcopy-GRP/interactive calling)
Organising bespoke Team/Client/Corporate related Events incl Field Trips
Understanding the teams strategy & required deliverables
Liaising with Corporates and Clients as and when required by analyst
Maintaining an invite & attendance log
Inception through to execution
Corporate Events & Roadshows
Liaising with the Corp Events & Roadshow depts. on behalf of the team
Ensuring that the event is appropriately branded
Work with teams to prioritise 1:1 meetings & target list
Product
Assist the team with all �branding� initiatives
Create & update bespoke marketing packs/presentations using Powerpoint
Assist with formatting Research product using our in house template and styles
Create, update and/or format tables, charts, diagrams for inclusion in Research product
Maintain up to date disclosures within company models and presentations
Other items to include but are not limited to
Comprehensive understanding of all Research Systems in order to be the �Go To� person for the team
Registering analysts for conferences & company days
Ensure Dealogic (Event Manager) is up to date with regard to client meetings pre event
Ensure Client Portal is up to date with meeting feedback post event
�Gate keeper� for team calendar, ensuring the appropriate meetings/details are recorded and maps / directions are provided where required, as well as company reporting dates
Booking point to point team travel, providing the relevant business justifications for approval
Complete understanding of the in-house T&E policy & procedures
Claiming analyst expenses and reconciling their American Express statements on a trip by trip basis
Answering phones for team � accurate message taking and problem solving where needed
Arranging ad hoc cars and couriers
Maintaining company contacts/client database and email/voicemail/mailing /calling lists etc(s)
Provide cover to the department during periods of holiday/absences and in times of heavy work flow
Timely and accurate filing (electronic & hardcopy) of research and company information
Any general administrative duties
Previous Equity Research experience desirable but not essential
Previous, client facing dept/role strongly desirable
Forward thinking and proactive approach to role & responsibilities
Proven ability to produce work quickly and of high quality
Ability to manage and develop new projects whilst maintaining quality across existing ones
Team player who�s engaged in the business and has a high level of attention to detail & accuracy
Confidence using Excel (charts, basic formulas)
Strong presentation skills using Powerpoint (creation as well as updating)
Strong communication (written and verbal) skills
Use to working in a demanding, fast-paced environment
Good use of initiative and self sufficiency in both busy and quiet times
A flexible approach to duties and ability to work longer hours when necessary (but not regularly)
Professional manner
Timeliness

Research Coordinator Resume Examples & Samples

Ensure appropriate correlation between focus/tiered accounts & distribution lists
Liaising with Corporates and Clients
Assist the team with all 'branding' initiatives
Assist with formatting Research product
Comprehensive understanding of all Research Systems in order to be the 'Go To' person for the team
'Gate keeper' for team calendar,
Booking point to point team travel
Claiming analyst expenses
Maintaining company contacts/client database and email/voicemail/mailing /calling lists etc
Timely and accurate filing of research and company information
Team player who's engaged in the business and has a high level of attention to detail & accuracy
Confidence using Excel and Powerpoint

CO OP Product & Research Coordinator Resume Examples & Samples

Ensure a high level of client service by
Responding to client requests and inquiries in a timely, responsive manner
Remaining up to date with all policies, procedures and regulatory rules as they relate to client accounts
Ensuring accounts are accurately documented and compliant with regulatory requirements
Maintaining client files and information
Proactively contacting clients to schedule advisor appointments
Researching client contact information in the event that the National Branch has not been informed by client of address or phone number changes
Ensure effective client administration by
Following up with clients on missing documentation required
Maintain activity logs including, but not limited to call logs, meeting logs, mail logs, etc
Coordinate client mailings related to changes in advisor or requests for client contact
Resolving issues expeditiously and accurately, escalating issues to Advisor or Manager when appropriate
Issuing instructions for client withdrawals, deposits, and transfers according to client or Advisor instructions
Ensuring all client interaction is accurately documented
Understanding the required documentation for all client account types
Supporting the growth of the branch by
Identifying opportunities to close unprofitable accounts and facilitating the closure
Reviewing processes to improve administrative efficiencies
Identifying opportunities to gather additional assets and/or increase revenue within the existing client base (i.e. referrals, consolidation of assets, insurance, etc.)
Retaining key clients by effectively communicating the National Branch value proposition
Providing recommendations for improvement to business processes, additional value to clients, and utilization of our Team of Experts
Contribute to the effective functioning of the branch team by
Supporting data analysis and management reporting functions
Building effective working relationships across the team and with various business line and corporate function contacts
Maintaining a high level of customer service
Facilitating a culture of open and honest communication
Actively participating and contributing to touch bases and team meetings
Encouraging the generation of new ideas and approaches
Actively sharing knowledge and experience to enhance the development of all team members
Developing and executing a meaningful employee development plan
Pleasant telephone manner and an ability to keep client conversations on track
Working knowledge of mutual funds
Working knowledge of investment and retirement planning sufficient to meet the needs of clients and to compete for the business within the current market
Strong MS Excel skills
Ability to take initiative and work independently
Ability to meet deadlines, and targets
Understanding of industry and firm compliance regulations
Experience as an administrative associate or sales assistant an asset
Experience with Dataphile is an asset

Research Coordinator Resume Examples & Samples

Assists with organizing and scheduling assessments/tests/activities to meet research objectives and study protocol compliance. Communicates with study team personnel to ensure study procedures are followed and research is performed as described in protocol. Serves as contact for subjects, study personnel, Institutional Review Board (IRB) and study sponsor
Participates in assessing patient eligibility. Assists in coordinating study participant activities including recruitment, screening, orientation and correspondence. Schedules subject appointments, tests, and procedures coordinating with external providers as needed. Produces reports and other materials, as directed
Maintains accurate, complete and timely records, including source documents, consent forms, case report forms, protocol documents, and regulatory documents, as required by sponsor and institutional guidelines
Assists with submission of timely, accurate, and complete study continuing review, amendments, and reportable events to IRB
Assists with sample collection, processing and shipment for each study

Research Coordinator Supervisor, CRS Resume Examples & Samples

10% Supervises and coordinates all aspects of sponsor-initiated and investigator initiated research studies including subject recruitment, data collection, scheduling of study-related assessments and follow-up of enrolled subjects, and budget development and administration. Plans and staffs project operations based on proposed research activities and timelines
10% Supervises staff engaged in sponsor-initiated and investigator-initiated research studies. Recruits screens, and hires staff. Performs performance evaluations and provides guidance and feedback to assigned staff. Counsels, disciplines and/or terminates employees as required
10% Schedules assigns, and prioritizes workloads on a daily basis. Sets appropriate goals and deadlines. Ensures timely completion of unit’s work. Assigns and monitors progress on work assignments and special projects. Trains and demonstrates techniques or procedures to research coordinators
9% Oversees the planning, organizing and scheduling of assessments/tests to meet research objectives and study protocol compliance. Communicates with study team personnel to ensure study procedures are followed and performed as described in protocol. Serves as primary contact for subjects, study personnel, Institutional Review Board (IRB) and study sponsor
5% Develops and manages internal budgets as required. Authorizes expenditures and monitors reconciliation and status to ensure compliance with fiscal guidelines and regulations. Prepares and/or directs the preparation of financial reports as required. Directs ongoing purchasing activities for supplies and equipment including authorization of one-time major purchases under supervision of supervisor. Researches new equipment purchases and develops recommendations for supervisor’s consideration
5% Assists in recruiting subjects for studies and determines eligibility based on study criteria. Coordinates and monitors study participant activities to include recruitment, screening, orientation and correspondence. Schedules subject appointments, tests, and procedures coordinating with external providers as needed. Produces reports, correspondence and other materials, as needed
5% Has responsibility for overseeing data collection for research studies following established data collection and management procedures. Oversees collection, recording, entering and preparation of data for analysis. Performs basic and moderately complex study analysis under the direction of Principal Investigator. Oversees the collections of pertinent information from study participants through interviews, administration of tests or surveys or questionnaires, medical records review, or other collection procedures
5% Oversees and ensures maintenance of accurate, complete and timely records, including consent forms, source documents, case report forms, protocol documents, and regulatory documents, as required by sponsor and institutional guidelines
5% Supervises the preparation and coordination of the submission of timely, accurate,

Research Coordinator Resume Examples & Samples

Creating and updating the experiment schedule while coordinating with a team of experimenters. Scheduling subjects for appointments and explaining study details and data collection procedures
Collecting MRI, EEG, and behavioral data with child participants, following established data collection and management procedures to prepare, collect, record, or enter data
Organizing and editing and maintaining datasets, while keeping accurate and detailed records
Collecting pertinent information from study participants through interviews, administration of tests, surveys, or questionnaires. Interview data will be recorded on paper and electronic forms as well as video
Have experience working in a research study environment
Have excellent written and verbal communication skills
Have excellent problem solving skills
Work well as a member of a research team
Be able to work independently and take initiative
Have the ability to interact well and engage with children and families from the USC community

Research Coordinator, CRS Resume Examples & Samples

Has responsibility for data collection for research studies following established data collection and management procedures. Collects, records, enters and prepares data for analysis. Performs basic study analysis under the direction of the Principal Investigator. Collects pertinent information from study participants through interviews, administration of tests, or surveys, or questionnaires, medical records review, or other collection procedures
Assists with development and management of project budgets. May authorize expenditures, monitor status and reconcile budget to ensure compliance with fiscal guidelines and regulations. Prepares and/or directs the preparation of financial reports as required. May direct ongoing purchasing activities including authorization of one-time purchases with approval from investigators
Organizes and prepares grant proposals. Collaborates with investigators to develop research proposals. Interfaces with funding and regulatory agencies to exchange information
Collaborates with pharmacist or materials management personnel to maintain accurate accountability of investigational products and specimens
Maintains automated databases and other records for reporting and compliance purposes. Generates reports and analysis of data according to project schedules or on an ad hoc basis. Provides guidance and direction to less experienced research coordinators in these efforts
Orders supplies and equipment. Researches and develops recommendations for new equipment purchases

Field Research Coordinator Resume Examples & Samples

Identify existing and potential sites and examiners, including but not limited to, searches in the system database, internet searches, and call lists that meet project criteria, communicate knowledgeably about current and/or forthcoming projects in order to elicit their participation in the project
Complete all follow-through tasks associated with bringing a site and/or an examiner on board including, but not limited to, developing letters and emails, overseeing distribution of specific project materials, and handling agreements within 24 hours of contact
Develop and maintain a relationship with sites and examiners, in order to communicate the populations, numbers, and validities required for each respective project
Maintain contact with sites and examiners on a bi-weekly basis, dependent upon project needs and maintain a record in the system
Fill portion of the sample assigned on time
Understand the sampling matrix and assign cases that fill the requirements in the sample
Work with sites/examiners to resolve any issues related to test protocols. Ensure sites/examiners are given correct and timely feedback on tested cases. Acquire product knowledge for all projects assigned to assist in study assignment
Ability to accurately enter data and all pertinent information related to each test protocol, utilizing various internal programs implemented to facilitate test tracking
Research and respond to inquiries from internal/external customers. Notify Manager of impact of requests
Create restricted-use web sites for communicating with participating sites (e.g., Word Press, Google sites, Blog Spot) and keeps these sites updated as the project progresses
Background in Marketing, customer service, or recruiting
Self-motivated, after training can work independently while seeking feedback from supervisors
Moderate to advanced proficiency in Excel/Word/Access/Power point
Comfortable with web technologies
Good phone etiquette

Senior Research Coordinator Resume Examples & Samples

Customer Service
Provide quality frontline customer service representing EY in a positive and professional manner
Coordinates the disposition and/or resolution of client issues
Supervise the work of employees in supporting roles, including assigning workload and reporting on employee performance
Administrative Support
Provide general administrative assistance
Support BD initiatives (researching key targets, planning email campaigns, scheduling meetings, preparing marketing materials),
Process client engagements in accordance to EY Policies and Procedures,
Provide assistance and support to the Project Manager in problem solving, project planning and management, and development and execution of stated goals and objectives
Assists in the coordination, supervision, and completion of special projects, as appropriate
Performs miscellaneous job-related duties as assigned
Strong interpersonal and communication skills and the ability to work effectively with a multi-disciplinary team
Ability to gather data, compile information, and prepare reports
Ability to use independent judgment and to manage and impart confidential information
Ability to analyze and solve problems
Ability to plan, develop, and coordinate multiple projects
Skill in examining and re-engineering operations and procedures, formulating policy, and developing and implementing new strategies and procedures
Skill in organizing resources and establishing priorities
Ability to lead and train staff and/or students
Knowledge of office management principles and procedures
Skills in the use of database management, word processing, spreadsheet, and/or presentation software
Organizing and coordinating skills
Ability to foster a cooperative work environment
Strong commitment to organizational goals and customer service
Initiative and Enthusiasm: Take self-directed action to do the job well. Anticipate potential problems and initiate corrective actions to avoid them

Research Coordinator Resume Examples & Samples

Expert level proficiency with media related software including OSi, AdConnections, Media Audit, KANTAR Media, Google Analytics or other comparable software
Must be able to effectively position and sell local broadcast affiliates with creative research and out of the box thinking
3-5 Years of experience working inside a small to mid-size meter-diary or local people meter market

Research Coordinator, Research Solutions Resume Examples & Samples

60% - Schedules appointments, makes travel arrangements, handles messages, expense reports and other administrative support
35% - Provides support for departmental projects and back-up for research managers as needed. Track and maintain dept invoices and budgets
5% - Coordinates department events

Research Coordinator Resume Examples & Samples

Provide research support for the Office of the President
Research topics relevant to DATG businesses, the media industry as a whole, and a wide array of current pop culture topics and issues
Help execute special projects and events by providing a variety of tasks as needed
Write briefs, memos, talking points and help prepare presentations for the office of the president
Draft various forms of communications on behalf of the office of the president
Communicate professionally in person, by phone, and through correspondence with a wide variety of DATG internal and external contacts on behalf of the Director, Office of the President
Provide daily administrative support including answering phone calls, scheduling meetings, managing travel arrangements, and T&E report processing
1-2 years administrative experience
Professional, poised, and possess outstanding written and verbal communication skills
Dynamic and critical-thinking mindset
Avid consumer of TV and media
Skills and experience interacting with social media
Demonstrated ability to handle confidential and sensitive information
Strong computer skills in MAC and Microsoft Office products, Word, Excel, and Outlook
Meticulous, attentive to detail, organized, approachable and friendly
Willingness to work non-standard, flexible work hours and overtime as needed; ability to serve in an “on-call” capacity
Ability to function with flexibility in a demanding environment with competing and changing priorities
Demonstrates the ability to assume responsibility without direct supervision; problem-solving skills
Ability to handle multiple concurrent tasks with frequent interruptions
Positive and committed approach to working with others to support team goals
Bachelor’s Degree or equivalent work experience

Field Research Coordinator Resume Examples & Samples

Bachelor's degree required, preferrably in a social science such as psychology
Background in marketing, recruiting, test development, and/or research & development
Ability to work evenings and weekends as needed

Research Coordinator Resume Examples & Samples

Job Summary: The Research Coordinator II assists the PI with formulating research objectives, contributes to design of research protocols, oversees clinical research trials, conducts quality assurance reviews. Provides assistance to PI in completing IRB and TRUE 2 and On-Core submissions. Coordinates fellows and residents who are working on research with the PI. Participate in investigator meetings as requested by PI
Clerical Summary: The Research Coordinator II develops clinical protocols, drafts and submits protocols for institutional review board (IRB) approval, develops informed consent forms, submits grants to funding agencies and potential corporate sponsors, develops grant budgets, maintains research accounts for clinical research projects. The Research Coordinator II communicates with collaborators in other departments and at other institutions. The Research Coordinator II develops and implements operating policies, procedures, systems and algorithms to support planned operations and ensures these are well-documented and communicated to project personnel. Prepares technical reports and papers on study plans, progress and results of research activities
Clinical Summary: The Research Coordinator II obtains informed consent from subjects, completes demographic data collection from subject, assists the investigator in collecting data during endoscopic procedures, assists the PI in “blinding” data for collaborators inside and outside the institution, maintains data base, de-identifies data prior to transmission to outside institutions
Managerial Summary: The Research Coordinator II interacts, oversees and otherwise leads a team of up to ten physician investigators working with the PI on a variety of clinical trials in a variety of settings. The Research Coordinator II presides over meetings of research staff, may organize research retreats or symposia, assists physician scientists with presentation of data at local, regional, or national meetings (including assisting in designing poster presentations or PowerPoint presentations)
Proven minimum 2 years experience in clinical research monitoring. Sound knowledge of all aspects of the clinical research process including but not limited to study design, start-up/closeout activities, regulatory requirements, data management
Experience in clinical research trials and trial protocol development. Knowledge of clinical trials components including statistics, study methodology, informed consent, eligibility, and adverse events. Success and skill at researching, analyzing, and evaluating information for preparation of clinical research protocols
Minimum 2 years experience in supervising and managing others with ability to set and meet goals, motivate others and hold individuals accountable for deliverables. Proven project management experience including forecasting, planning, and initiating action for successful project completion

Market Research Coordinator Resume Examples & Samples

Excel at paying close attention to detail
A self-starter who works well independently and can navigate within a large company with complex systems
Ability to synthesize and analyze data and share findings
Expertise with Google and Microsoft Office Suite and SurveyMonkey
Requires 2 years of full-time experience in addition to a post-secondary degree
Prefer experience with SPSS or other statistical programs
Prefer experience with video editing programs

Research Coordinator Resume Examples & Samples

Ensures that study is conducted as written so that scientific questions are answered
Conducts ongoing assessment of protocol deviations and violations
Participates in NCI, FDA and pharmaceutical audits and is knowledgeable of their regulations, especially concerning the reporting of Serious Adverse Events. Enters SAE into iStar for reporting to the IRB. Notifies Data Managers promptly of occurrence of SAE
Interacts with the monitors/auditors from the sponsoring pharmaceutical companies

Field Research Coordinator Resume Examples & Samples

Identify existing and potential examiners and sites, including but not limited to, searches in the system database, internet searches, and call lists that meet project criteria, and communicate knowledgeably about current and/or forthcoming projects in order to elicit their participation in the project
Complete all follow-through tasks associated with bringing a site and/or an examiner on board including, but not limited to, developing letters, overseeing mailing of specific site and examiner project materials, and handling agreements within 24 hours of examiner contact
Develop and maintain a relationship with examiners, in order to communicate the populations, numbers, and validities required for each respective project
Maintain contact with examiners on a bi-weekly basis, dependent upon project needs and maintain a record in the system
Bachelor’s Degree in Psychology, Education, Sociology, Communication, Business, or other closely related degree. Some Master's coursework preferred
Marketing, customer service, psychology, or recruiting background. Prior experience in a school or clinical setting working with assessments is preferred
Moderate to advanced proficiency in Excel/Word/Access. 1 year or more experience working with large databases (SQL, Oracle, etc) is preferred
Professional demeanor to identify and recruit examiner/sites
Positive, can-do attitude

Information & Research Coordinator Resume Examples & Samples

Track and process daily tax news for the purposes of posting to the Internet and converting to Folio. This material includes legislation, news releases, budget materials, and administrative materials (bulletins, guides, etc.)
Work with content files to manipulate their format and structure for electronic (DVD and Internet) publication
Provide administrative support for EY’s Tax practice knowledge databases and applications, as required
A post-secondary degree or diploma
Strong proofreading and writing skills
Practical knowledge of any of the following is a plus: Folio Views, Adobe FrameMaker, HTML
The ability to meet deadlines and process material efficiently
Excellent attention to detail, strong organizational skills, and flexibility
A high degree of comfort learning and applying new technology
Excellent interpersonal skills; the ability to communicate effectively, work in an office environment, and deal with clients, colleagues, and government sources professionally and effectively
Bilingualism is a plus

Research Coordinator Resume Examples & Samples

Assists with organizing study related activities to ensure compliance with FDA, GCP, IRB, HIPAA, SOPs, sponsor and institutional regulations and requirements. Serves as contact for subjects, study personnel, the department, the school, pharmacy and other ancillary service departments, Institutional Review Board (IRB) and study sponsor
Participates in assessing patient eligibility. Assists in coordinating study participant activities including recruitment, screening, orientation, correspondence, and ongoing patient education about clinical trials. Schedules subject appointments, tests and procedures with internal and external providers as needed
Assists with data collection, input, and analysis for research studies. Maintains accurate, complete and timely records, including source documents, consent forms, case report forms, protocol documents, and regulatory documents, as required by sponsor and institutional guidelines
Assists with sample collection, processing and shipment for each study. Orders supplies and equipment. Researches and develops recommendations for new equipment purchases
Assists in organization and preparation of grant proposals. Gathers documentation such as annual reports and detailed budgets for inclusion in proposal. Assists investigators in developing research proposals. Interfaces with funding and regulatory agencies to exchange information

Oncology Clinical Research Coordinator Resume Examples & Samples

5+ years of nursing experience
CT licensed RN
BSN and OCN certification
Knowledge of current nursing/medical practice in Oncology
Ability to coordinate & oversee adherence to clinical trial protocols
Detail-oriented with good organization skills
Critical thinking, work independently, computer proficiency are musts
Familiar with contracts and budgets associated with trials $

Research Coordinator Resume Examples & Samples

Bachelor’s degree minimum educational qualification
Experience in learning science, publishing or education, or in market research positions in other industries or education
Experience in dealing with customers an advantage

Research Coordinator Resume Examples & Samples

Vehicle might be required; home visits are located ~10-20 miles from the Texas Medical Center in Houston, TX or surrounding Houston area
Excellent ‘people person’ with ability to interact and communicate effectively with mothers of infants
Must enjoy working with young infants
Skills in handling infants required
Self-directed work style and high level of motivation
Passionate about child development and child psychology
Learn and adapt quickly to changes
Work well under pressure
Proficient using a computer
Prior experience with computer spreadsheets and database management

Research Coordinator Resume Examples & Samples

Collects and enters data into study database
May coordinate and schedule research subject appointments for tests and procedures
Maintains records for clinical study and regulatory documents
May correspond with patient throughout study
Composes and types study correspondence and other documentation
May recruit, advertise,and screen for research patients
May assist in determining patient eligibility for research protocols
Performs other job related duties as assigned

Research Coordinator Resume Examples & Samples

Recruit, inform and consent parents and parent-child dyads to participate in studies
Set-up, initialize, collect, download and clean accelerometer (activity monitor) and GPS data from data collection
Responsible for survey questionnaire data entry; merging of survey and accelerometry/GPS data; and maintaining the study databases
Manage and supervise research assistants hired for the study, including developing training materials for research staff and providing face to face training prior to study start
Perform related tasks as required to complete the research protocols, including creating research study forms, databases and other tools as appropriate
Upload confidential participant data from devices such as PDAs, GPS monitors, and activity monitors, report research findings, work with multiple types of research collection forms, independently develop and maintain Microsoft excel spreadsheets and access databases and demonstrate proficiency with outlook email communication and documentation
Assist with administrative duties of research study such as audit preparation, prepare study reports, management of research budgets, monetary disbursements, complete expense reports and organize participant files
Network and collaborate with organizations in the community for recruitment purposes
Ensure research projects are managed and completed according to agreed timelines, recruitment goals and quality standards
Experience working with children, preferred
Knowledge in conducting heights, weights, GPS and CSA measurements, behavioral, and physical activity questionnaires helpful
Willingness needed to travel within Houston area and work some evenings or weekends
Skill and comfort with using PC computers including Word, Excel, Access, PowerPoint, and Survey Monkey (or equivalent) software programs a must
Excellent communication skills, both oral and written, and interpersonal skills with investigators, staff, and participants (parents and children)
Great people interaction skills to work in community to recruit participants
Precision in preparing physical activity materials, recording data, protocol documentation, and data entry
Knowledge of study methods and procedures
Flexibility and adaptability in work schedule and carrying out job duties, including possible evening and weekend hours
Fast learner, great organizational skills, resourceful, and capable of multi tasking
Decision making skills, problem solving skills and leadership skills
Detail oriented and ensures tasks are completed correctly and on time
Bilingual in Spanish a plus
Must have a car or other ways of getting to families homes and community study sites around Houston, Texas, as work is performed at the Children’s Nutrition Research Center (CNRC) and various neighborhoods in Houston
Must be able to lift and move required assessment and physical activity equipment and materials
Will take part in trip validation studies around Houston and may make home visits for data collection paired with another study staff in the future

Research Coordinator Resume Examples & Samples

Attend and pass BCM certified training on HIPAA and human subject research and consent procedures
Responsible for recruiting, informing and consenting parents and parent-child dyads to participate in studies
Computer proficiency required including, but not limited to, uploading of confidential participant data from devices such as PDAs, GPS monitors, and activity monitors, reporting of research findings, working with multiple types of research collection forms, independently developing and maintaining Microsoft excel spreadsheets and access databases and demonstrate proficiency with outlook email communication and documentation
Assist with administrative duties of research study such as audit preparation, assisting in preparing the study reports, management of research budgets, monetary disbursements, completing expense reports and organizing participant files
Networking and collaborating with organizations in the community for recruitment purposes
Ensure that research projects are managed and completed according to agreed timelines, recruitment goals and quality standards
Education Required: B.S. in exercise physiology, kinesiology, public health, health psychology or related field, required
Education Preferred: Masters degree with two years of work experience in field of physical activity research
Experience Required: One year of relevant experience in a research setting with Bachelor degree or Five years of relevant experience in a research setting without a Bachelor degree
Experience Preferred: Experience working with children, preferred
Preferred: Bilingual in Spanish a plus
Computer literacy with prior experience with Word, Excel, Access, PowerPoint, Survey Monkey (or equivalent)
Supervision: Supervised by Project Investigators and Co-Investigators
Working Conditions: Must have a car or other ways of getting to families homes and community study sites around Houston, Texas, as work is performed at the Children’s Nutrition Research Center (CNRC) and various neighborhoods in Houston
Physical Requirements: Must be able to lift and move required assessment and physical activity equipment and materials
Physical Risk: Will take part in trip validation studies around Houston and may make home visits for data collection paired with another study staff in the future

Research Coordinator Resume Examples & Samples

Collects and documents research data
Maintains records for clinical study and regulatory documents May recruit, advertise, and screen for research patients
Enters study data into a computerized database or case report form
May schedule research subject appointments for tests and procedures, such as laboratory tests, x-rays, and other studies specific for the research protocol
Retrieves and submits test results to appropriate party
Education Required: Bachelor Degree in a related field; Four years of relevant work related experience in a research setting can be substituted in lieu of a degree

Research Coordinator Resume Examples & Samples

Executes research visits as designated by specific protocol guidelines. This includes identifying subjects scheduled for clinic visits or hospitalized patients potentially eligible for enrollment and preparing for study visits (scheduling research visits, preparing documentation for visits, submitting laboratory orders, contacting subjects before visits, working with physicians and nurses and other personnel involved in study visits)
Conducts all testing procedures required by research coordinator as delineated in the study protocols and Manuals of Operations
Evaluates and formats clinical research data and transmits it to central Data Coordinating Center
Regularly communicates with Data Coordinating Center and responds to data queries and other requests
Coordinates with the pathology department and interventional radiology department in procuring and appropriately processing and shipping human specimens (tissues, serum/plasma, DNA)
Prepares documentation and obtains data necessary to obtain initial and continued approval for applicable research protocols. Screens for and recruits research subjects
Conducts patient interviews to evaluate patient eligibility in studies and conducts interviews as part of routine study visits
May work with research pharmacy in procuring study medications for enrolled subjects
Prefer fluent Spanish
Must be able to multi-task and meet timeline goals
Most important qualifications are good interpersonal skills, high attention to detail, team-goal oriented, ability to stay well organized, and ability to effectively communicate orally and in writing with study subjects, research personnel and caregivers
Must be computer literate and have experience using Microsoft Office software

Research Coordinator Resume Examples & Samples

Required: Bachelor's Degree in a related field; four years of relevant work related experience in a research setting can be substituted in lieu of a degree
Required: Two years of relevant experience in a research setting with Bachelor's degree or six years of relevant experience in a research setting without a Bachelor's degree
Preferred: Experience in oncology studies
Bilingual (Spanish/English) is a plus
Certification as MA or NA is a plus
Certification in GCP is a plus
Must be able to communicate effectively, both verbally and in writing
Experience with computer spreadsheets and database management
Ability to understand patient studies and protocols
Data entry and knowledge of electronic medical record keeping

Research Coordinator Resume Examples & Samples

Coordinates with the operating room, pathology department, and or interventional radiology department(s) in procuring and appropriately processing and shipping human specimens (tissues, serum/plasma, others)
Prepares documentation and obtains data necessary to obtain initial and continued approval for applicable research protocols
Screens for research subjects or, less commonly, may recruit and advertise for them
Must be computer literate and have experience using Microsoft Office software. Preferable to have experience using EPIC database for patient care records

Senior Research Coordinator Resume Examples & Samples

Plans and organizes research protocols as designated by specific protocol guidelines
Conducts testing procedures required by study protocol
Participates in designing surveys used in study protocols
Documents results of study data and reports to principal investigators
Performs literature searches and prepares literature reviews
May recruit, advertise, and screen for research patients
May conduct patient interviews to evaluate patient eligibility in study. S
Supervises, schedules and directs the activities of less experienced research personnel

Senior Research Coordinator Resume Examples & Samples

Some of the responsibilities include accurate data collection, documentation, organization, oversight of the safety of study volunteers, and communication with volunteers’ families
Oversees local regulatory (IRB) requirements and maintains close communication with extramural study investigators, pharmaceutical sponsors and Therapeutic Development Center
Assists the investigator in the overall conduct of clinical trials as assigned
Ensures conduct of assigned studies is in accordance with good clinical practice, federal regulations and institutional policies
Communicates verbally and in writing as needed or as requested by the principal investigator of the study
Participates in protocol feasibility assessment and actively participates in protocol meetings including but not limited to investigator and site initiation meetings
Assists in training other support staff in study coordination
Participates in protocol monitoring, audits and follow up in coordination with other research staff
Maintains contact with other institutions participating in the studies
Prepares study related tools and assist principal investigator in reviewing treatment and visit order sets
Interacts with sponsors as required to facilitate protocol activities and maintain current study documents
Conducts research subject recruitment, screening, and enrollment
Conducts subject interviews to evaluate eligibility and continued participation in the study
Participates in subject consent process
Performs research related procedures as required (e.g.: blood draw, ECG, EEG, spirometry, sweat testing, questionnaires, etc.)
Conducts subject research study education as required within the scope of practice
Develops and maintains a processing and tracking system for all paperwork
Submit serious adverse event reporting and follow up as needed
Evaluates and analyzes clinical research data as appropriate
Interacts with patients to clarify data

Senior Research Coordinator Resume Examples & Samples

May conduct patient interviews to evaluate patient eligibility in study
Education Required: Bachelor's degree in a related field or four (4) years of directly related work experience in lieu of a degree
Experience Required: Five years of relevant experience in addition to any educational requirements

Development Research Coordinator Resume Examples & Samples

Master's degree and three years of professional experience in fundraising, communications, program management or a related function
Professional experience in a complex fund raising, communications, or program management role
Development experience in a complex institutional environment such as a university or other large organization is desirable
Sophisticated project management, organizational, and communications skills
Ability to stay on top of multiple complex projects
Ability to communicate confidently and professionally with a wide variety of constituents, including university administrators, donors, development and institute leadership, and colleagues
Flexibility to handle ad hoc assignments and accompanying deadlines
Demonstrated familiarity with corporate and foundation philanthropy in policy work (in an organization such as an advocacy organization, think tank, or academic public policy school/department/center)
Familiarity with key issues and decision-making processes in public policy, with interest or experience in environmental issues a plus
Good judgment in handling sensitive and confidential information and issues on a routine basis

Assistant Clinical Research Coordinator Resume Examples & Samples

Familiarity with Autism and Learning Disabilities resources in the Bay Area
Basic computer skills and demonstrated experience with office software and email applications
Ability to follow through and complete assigned tasks

Assistant Clinical Research Coordinator Resume Examples & Samples

Prior clinical or research experience, including undergraduate experience
Strong proficiency in Microsoft Word and Excel
Demonstrated ability to work independently with minimal supervision, as well as cooperatively in a team environment
Excellent organization, communication, and problem-solving skills
Ability to work effectively with a wide range of individuals and groups at all levels of authority
A proven capacity to set priorities, coordinate multiple assignments, work in a fast-paced, multi-tasked environment, exercising sound judgment in setting priorities with a strong attention to detail
Experience working with health care professionals and clinical research participants

Assistant Clinical Research Coordinator Resume Examples & Samples

Knowledge of Epidermolysis bullosa
Experience working with children and families dealing with complex medical conditions
Bachelor's degree in a related field or an equivalent combination of related education and relevant experience

Clinical Research Coordinator Float Replacement Resume Examples & Samples

Strong organizational skills and a demonstrated ability to work independently with minimal supervision as well as cooperatively in a team environment
Bachelor's degree in a related field or an equivalent combination of related education and relevant experience required
One year of relevant experience desired

Research Coordinator Resume Examples & Samples

Coordinate D & L Fellows staff acquisition activities—development of job descriptions, interview to hire process, including VU Hire-A-Dore specifications and coordination with Dr. Nwankwo, the English Department’s Administrative Assistant and WWG Research Project Coordinator
Supervise all Discovery & Learning Fellows working across all projects
Monitor activities and provide guidance to D & L Fellows Coordinators on all WWG Projects
Maintain regular contact with Lead Organizer, Lead Collaborators, faculty, staff, D&L Fellows and external collaborators by email, telephone, text messaging, web conferencing or Project Based software
Create, manage and monitor team activities on a project software application (Basecamp) or other project management application to assure benchmarks are achieved according to the project timeline
Provide verification of all D & L Fellows completed assignments for Approvers of the D & L Fs ETimecard submitted to VU Student Employment Services
Monitor financial procurement documentation and financial reports to ensure there are no budget overruns, working in conjunction with the English Department’s Administrative Assistant and Dr. Nwankwo
Provide oversight and maintenance of the Cloud storage files, physical files, materials, other documentation and product deliverables by curating, collecting, compiling, and organizing data in conjunction with the D & L Fellows, Dr. Nwankwo and other relevant individuals
Coordinate/manage meetings (In-person, teleconferences, web-based conferencing) for all project collaborators, internal and external in conjunction with Research Assistant
Coordinate all logistical aspects for planning public events and exhibitions in conjunction with the D & L Fellows, Dr. Nwankwo, and other relevant individuals or organizations
Write monthly Progress Reports and other reporting to communicate projects progression or issues
Coordinate accessibility to historical project files, documents, materials
Proposal coordination – administering proposal process in conjunction with Dr. Nwankwo and other relevant individuals
Other Administrative tasks: Financial report monitoring, D& L Fellows tasks/hours worked verification, supplies and materials procurement, travel coordination, community relationship building activities and other reasonable tasks assigned by the Lead Organizer
Submit invoices for payment of services from external individuals, vendors, contractors to Vanderbilt University Procurement Services monthly

Research Coordinator Resume Examples & Samples

Assisting in diverse ways with the analysis and presentation/communication of social science research to a broad array of audiences
Updating the content and interface of the research project’s website
Advising and assisting in the development of public relations and social media strategies for the dissemination of results and to connect with broader audiences
Managing subscriptions to and helping to grant access to LAPOP data
Sending reports by email and regular mail to project supporters, libraries, and others
Conducting descriptive analysis (percentages, means, cross tabulations), along with the production of graphs to describe data for placement in press releases, on websites, and in other communications
Working independently and with Vanderbilt’s Creative Services to generate infographics and other visual representations of data for reports, social media, and the web
Proofing and editing of reports and presentations, especially those directed toward policy makers, the general public, and the media
Writing press releases in both English and Spanish in collaboration with the Vanderbilt news and communications office
Creating internal reports, managing and cataloging project files
Assisting with the day to day administrative operations of the LAPOP research unit
Bachelor's degree and 5 years of experience or the equivalent required. Master’s in communications (journalism), public policy, or the social sciences preferred
Ability to write and communicate clearly and accurately in both English and in Spanish is required
The ability to understand and communicate about social science research is important
Knowledge of statistical analysis and software is a plus
Familiarity with Windows, Excel and Word is required
Familiarity with web design, social media techniques, and press release development is essential
Willingness and ability to travel domestically and abroad, only on occasion and for short periods of time (generally no more than 1-2 days) to carry out tasks related to research outreach

Clinical Research Coordinator, Senior Resume Examples & Samples

Master’s degree in a field appropriate to the area of assignment AND three years related research experience; OR, bachelor’s degree in a field appropriate to the area of assignment and four years related research experience
Bilingual preferred (Spanish, Navajo/Diné Bazaad, other)
Previous human subjects training (e.g., CITI certification) and four years’ experience as a research coordinator with direct recruitment and enrollment responsibilities
Current Certified Clinical Research Professional (CCRP) status
Self-motivated, willing and able take initiative

Research Coordinator Resume Examples & Samples

Maintain the lab budget and purchasing records
Responsible for the overall operation and administration of the laboratory, including technical oversight of personnel
Review, conduct, provide and maintain all training records of laboratory personnel
Write, update, and maintain SOP manuals
Maintain compliance with NIH Public Access Policy
Maintain all biological, chemical, radiation, and laser safety audits
Handle all security documents
Schedule lab equipment use for staff and collaborators
Purchase/inventory lab supplies
Express active interest in independently learning scientific background and current research performed in the lab
Assist in preparation and publication of scientific manuscripts
Become proficient with the grant submission and update requirements
B.S. or B.A. degree
Ability to learn new online protocols for the submission and updating of grants
Highly motivated and organized in record keeping
Background and hands on experience in laboratory, veterinary, or clinical settings in regards to federal, state and university regulations
Background in supervising technical and non-technical staff
Creative thinking skills

Research Coordinator Resume Examples & Samples

Scheduling research activities
Presenting at conferences and workshops
Working with the Human Subjects Protection Program to ensure compliance with all human subjects requirements
M.A. in Special Education, Education of Deaf/Hard of Hearing (DHH) or related field
Ability to work with young DHH children
Proficiency in American Sign Language and English
Knowledge of language and literacy development in young children who are DHH
Demonstrated ability working in a team setting and/or with a team of researchers
Teaching Certification

Research Coordinator Resume Examples & Samples

Strong decision making ability
Time management and organization skills
Ability to prioritize and work with leadership to operationalize tasks
Strong computer skills and knowledge in lab information systems
Advanced proficiency in Microsoft Office, specifically Excel and Access
Excellent oral written communication skills
Experience in a research laboratory preferred
Experience with grant submissions and grant submission software
Experience preparing, tracking and managing budgets and financial reports

Research Coordinator Resume Examples & Samples

Oversee and contribute to the design study questions, protocol, and materials, including structured interviews, recruitment flyers, and data collection protocols
Coordinate study team in conducting 60 minute structured pre-, post- and follow-up assessments with study participants
Help establish, formalize, and maintain relationships with community organizations, hospitals, clinics, etc. for recruitment and collaboration
Oversee IRB application process for all project components and work with research team to ensure all IRB requirements are met
Oversee the hiring, training and supervision of student study assessment team
Deliver mindfulness-based stress and self-compassion intervention to study participants
Conduct and direct regular, ongoing communication of research team; develop meeting agendas; attend meetings and take and disseminate meeting minutes; ensure investigator and staff follow-up on assigned action items
Other duties, as assigned
Certified in delivering mindfulness-based child birth or stress-management program
A minimum of five years’ experience in psychology, public health or social sciences research, including experience in coordinating complex research projects
Demonstrated qualitative and quantitative analytical skills; experience conducting literature searches and preparing literature reviews; experience in data analysis using spreadsheet software, such as MS Excel
Demonstrated ability to describe research projects and represent projects and colleagues in a professional and congenial manner with professional colleagues within academia and within public and private organizations outside of academia. -Demonstrated oral presentation skills, both with and without Microsoft PowerPoint. -Excellent written communication skills
Experience working with members of community organizations
Experience in planning, organizing, and facilitating research team meetings to achieve specific objectives
Experience in planning and organizing large meetings of people from various professional backgrounds including setting meeting goals and objectives; developing meeting sessions designed to advance objectives for specific research projects; and ensuring that appropriate investigators and researchers are brought together for specific agenda items
Ability to work independently with limited supervision, and to work as part of a team. Ability to balance multiple demands simultaneously under time constraints
Ability to exercise sound judgment and to address complex situations with creativity
Ability to communicate well with people from diverse ethnic/racial and socioeconomic backgrounds
Highly organized and attentive to detail; ability to balance multiple demands simultaneously under time constraints
Proficiency in MS Word, Excel, and PowerPoint
Flexibility might be needed in work schedule due to the nature of two-state research project (California & Washington)

Research Coordinator Resume Examples & Samples

Collaborate with faculty to write and develop study protocols. Manages the approval and implementation of research protocols, and work with process partners to ensure all protocol requirements are met
Monitor patient adherence to the protocol by providing compliance and study calendars. Take action to correct problems such as deviation from protocol requirements and maintain all reporting requirements
Recruit and screen human subjects for the study
Collect all case report forms, patient charts, images, radiographs, pathology specimens, and other clinical data of human subjects
Administer Neurocognitive Tests and Quality of Life Questionnaires to the study patients per protocol requirements
Communicate with external patients and referring physicians who are interested in enrolling patients to the study. Provide timely and actuate information to all internal and external inquiries
Submit and maintain regulatory requirements of the trial, and protocols. Meet deadlines for amendments and annual reviews; issue reports for compliance and study deviations to all review boards, including the Institutional Review Board (IRB)
Oversee the required documentation for participation of all UW-affiliated medical institutions, such as investigator information, site certifications, annual accrual figures, and any other procedural requirements
Manage clinical research budget and track billing charges; ensure correct charges go to study as required; catalog and document review of charges to protocols as needed
Develop reports and maintain direct communication with faculty members, UW departments, funding sponsors, and research collaborators regarding study overall research plan
Help identify problems with clinical trial start-up and management. Assist with organized improvement efforts and developing research study design improvements
Works directly with faculty to design and improve data collection efforts. Manages all data collection
Collaborates and assists with investigators to write manuscripts, articles, abstracts and research reports for publication in peer-reviewed journals

Research Coordinator Resume Examples & Samples

Demonstrated success managing national, longitudinal human subjects studies
Experience with UW research and fiscal offices and proficiency with UW systems, including SAGE, Granttracker, MyFinancial Desktop, and Ariba
Knowledge of social media use for business and professional communication/marketing

Research Coordinator Resume Examples & Samples

Coordinates the implementation and conduct of research projects ensuring adherence to research protocol requirements including: timely completion and communication of regulatory documents, the development of data capture and monitoring plans, reporting of Serious Adverse Events as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP timelines
Collaborates with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols, including research subject recruitment
Completes regulatory documents, data capture and monitoring plans
Assists with preparation for audits and response to audits
Provides and documents education as needed
Minimum two years clinical research or healthcare experience required
Bachelor's degree in healthcare or science field may offset experience requirement
Demonstrated basic computer proficiency
Strong organizational, communication and interpersonal skills
Must be self-directed with demonstrated ability to work independently yet establish cooperative relationships with colleagues

Research Coordinator Resume Examples & Samples

Collaborate with study personnel in the planning and submission of grant applications for internal and external funding
Integrate information from multiple sources to ensure that research proposals meet the necessary requirements of funding agencies
Conduct literature reviews on topics pertinent to research protocols and strategic initiatives
Design, create and revise data collection tools in collaboration with principal investigator, statistician and data management team, and conduct data entry as needed
Coordinate quantitative and qualitative data collection efforts for one or more research projects, which may include other collaborating agencies or institutions
Manage research participant contact and report problems and concerns to principal investigator
Manage project timelines and prepare interim reports for principal investigators, industry sponsors and institutional review board to ensure timely completion of each project
Liaison between the project team and funding agencies or significant parties
Reviews applications for research projects to ensure that protocols meet regulatory and ethical standards for the protection of human subjects
Provides consultation services and acts as liaison to DA2 investigators, staff and students, on the application and implementation of the federal regulations, state laws, and CHS institutional policies for human subject research
Maintains IRB records, both in paper and electronic format, submission of IRB applications, amendments, procedural changes, and continuing oversight of compliance
Prepares presentation materials and delivers educational programs on regulatory and ethical compliance in research to DA2 investigators, staff and students

Research Coordinator Resume Examples & Samples

Research study participant recruitment, screening and enrollment
Schedules patients' appointments and appropriate testing for patients as directed. Verifies information from patients including demographic and health insurance information
Follow-up in accordance with specific protocol
Reports to the principal investigator any deviations of normal operations
Reports to the principal investigator any unusual occurrences related to research study participants, staff or equipment
Reports immediately any changes in the research study participant's condition warranting intervention
Maintains appropriate communication with study sponsor and referring physicians
Responsible for preparation and submission of protocols for Research/Human Subjects Committee (IRB) approval. The scope of the clinical trials includes evaluation of therapy, assessment of effect of treatment, ongoing evaluation and long-term assessment of comprehensive management program, and evaluation of the effects of risk factor modification program
Responsible for completion of pertinent data relevant to patient enrollment in clinical research studies/clinical trials and management of data from procedures performed
Demonstrates knowledgeable assessment skills while constantly monitoring the patient's status throughout the duration of the clinical research study/clinical trial
Assists the principal investigator in the evaluation, care and follow-up of research study participants
Maintains appropriate study participant research records and documentation
Shall be accountable for maintaining the confidentiality and security of all medical center related, clinical trial related, medical staff related and patient related data and information as per HIPPA standards
Shall be accountable for abiding by all relevant policies and procedures
Responsible for maintaining annual competencies, training, and certifications as required
Performs other related duties as requested
Ability to read, speak, write, and understand the English language
Ability to complete mathematical computations required to perform tasks
Strong interpersonal, organizational, and oral communication skills
2-3 years experience in a health care setting as a research coordinator or a comparable position
Experience with organization of medical charts preferred
Strong interpersonal and telephone skills required
Word-processing and computer data entry experience preferred
Typing skills must be a minimum of 30 wpm

Assistant Clinical Research Coordinator Resume Examples & Samples

Experience working in a Cancer Center and familiarity with members of Cancer Center team and patients
Familiarity with chart review and tracking relevant data from charts ; record data with extreme accuracy
Attention to detail and the ability to work effectively with a wide range of individuals and groups at all levels of authority
Experience with database software, MS Office

Market Research Coordinator Resume Examples & Samples

Facilitate departmental interactions with Procurement, including
Submit procurement requirements: Confidential Disclosure Agreements (CDAs), requisitions, and bid exceptions
Track requisition approval status, assignment of Purchase Orders (POs), and invoice payments
Track spend vs. budget for overall department as well as individual molecules and indications
Track secondary/syndicated subscriptions, user credentials, and renewal dates
Coordinate vendor site visits: introductions, capabilities meetings, and evaluations
Coordinate SurveyMonkey-type activities – documenting objectives and key questions, creating and fielding surveys, and summary of results, as needed
Ensure the following materials are posted to SharePoint in a timely manner: final project reports, relevant vendor contact info and capabilities presentations, team member status reports, and other materials, as needed
Process expense reports, as needed
Disseminate research travel logistics to attendees (dates, facility locations, and recommended hotels)
Maintain master department calendar and non-Regeneron partner contact list
Book internal and external meetings, including meeting invites, conference rooms, catering, directions, and security registration, as needed
Coordinate departmental staff meetings and communicate action items, next steps, and new topics
Coordinate internal collaboration meetings across Commercial and non-Commercial teams
Consistent coordination and communication with Commercial staff regarding workload balance and coverage, facilities needs and issues, and companywide activities
Basic administrative assistance as needed, including: management of travel needs, copying and printing of materials, coordination with shipping and receiving, presentation support

Assistant Clinical Research Coordinator Resume Examples & Samples

Familiar with excel
Ability to navigate web based databases
Strong interpersonal and organizational skills desired

Research Coordinator Resume Examples & Samples

Degree in business administration or related field
Proficiency in the use of MS Word, Excel, PowerPoint, Outlook. Experience with both Macintosh and Windows platforms a plus
Demonstrated ability to communicate with university students, faculty, administration, community program participants, community partners

Research Coordinator Resume Examples & Samples

Coordinates day to day activities of clinical research protocols
Ensures accurate data collection, documentation, organization and safety of study volunteers
Required: Three Years of relevant experience in a research setting without a Bachelor degree
No experience required if candidate has a Bachelor degree in a related field

Research Coordinator Resume Examples & Samples

Self-directed, independent and organized
Requires experience using Excel and knowledge of database management
Requires the ability to understand and implement patient studies and protocols
Prefer experience with specimen handling
Bilingual a plus

Research Coordinator Resume Examples & Samples

Responsible for recruiting, advertising, and screening for research participants. This involves identifying advanced cancer patients from the institutional database, coordinating with physician collaborators to contact patients and their family caregivers in the clinic for the purpose of recruitment, and registering study participants on the protocol. Recruitment may be exclusively at Baylor Clinic other sites in the Texas Medical Center depending on project needs
Collects and enters data into study databases
Supervision: Not normally required to supervise others
Customer Service: Takes routine or required customer actions to meet customers' needs. Responds promptly and accurately to customers' complaints, inquiries, and requests for information and coordinates appropriate follow up
Working Conditions: Generally, work is done in an office environment with pleasant working conditions. There is good lighting and ventilation, it is reasonably quiet, and the work hours are reasonably regular
Physical Requirements: Rarely required to exert physical effort
Physical Risk: Does not handle/work with biohazards or risks for potential job-related injuries
Required: One year of relevant experience in a research setting with Bachelor degree or Five years of relevant experience in a research setting without a Bachelor degree

Research Coordinator Resume Examples & Samples

Collect and document research data
Maintain records for clinical study and regulatory documents
Enter data into a computerized database or case report forms
May schedule research subject appointments for tests and procedures, such as laboratory tests for the research protocol
Retrieve and submit test results to appropriate party
May obtain specimens
Ship specimens
Correspond with patient throughout study
Order supplies and equipment
Work with multiple hospital information systems such as the VA EMR, EPIC, BRAIN and Access and Excel databases
Organize research protocols as designated by specific protocol guidelines and report to principle investigator
Perform other job related duties as assigned, including writing and reviewing drafts of manuscripts
Preferred: Masters in Public Health
Experience Required: Two years of relevant experience in a research setting with Bachelor degree or Six years of relevant experience in a research setting without a Bachelor degree

Assistant Clinical Research Coordinator Resume Examples & Samples

Excellent leadership and organizational skills with high attention to detail
Experience with and familiarity with Autism and Learning Disabilities resources in the Bay Area
Experience with recruitment of research participants for clinical studies, including contacting and visiting schools, working with children and adolescents in experimental settings, working with diverse populations, clinical interviewing and community outreach

Research Coordinator Resume Examples & Samples

Recruit, advertise, and screen for research patients
Conduct patient interviews to evaluate patient eligibility in the study
Schedule research subject appointments for tests and procedures, such as laboratory tests, x-rays, and other studies specific for the research protocol
Retrieves and submits test results to the appropriate party
Correspond with the patient throughout the study

Senior Research Coordinator Resume Examples & Samples

Required: Bachelor's degree in a related field; four years of relevant work related experience in a research setting can be substituted in lieu of a degree
Required: Five years of relevant experience in a research setting with Bachelor's degree or nine years of relevant experience in a research setting without a Bachelor's degree
Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) preferred
Bilingual, English and Spanish, is a plus and preferred

Senior Research Coordinator Resume Examples & Samples

Phlebotomy experience preferred
Bilingual, English and Spanish, is preferred but not required
Ability to communicate with patients, families, doctors, and other healthcare providers
An in-depth working knowledge of IRB requirements, FDA regulations, Good Clinical Practice, and ICH guidelines for the conduct of clinical trials
Must be conscientious, detail-oriented and be able to effectively manage multiple priorities concurrently
Coordinate and establish priorities among diverse tasks
Proper utilization of medical equipment and supplies and experience with specimen processing

Research Coordinator Resume Examples & Samples

Preparing policy briefs and summaries relating to short term rental legislation to present internally to staff
Daily monitoring of municipalities relating to relevant regulatory events
Short and long term tracking of local city governments current and future regulations
Providing comprehensive policy analysis on regulatory issues in markets including city codes, staff reports, and policy discussions
Meeting with regional policy managers and outside consultants to liaison with the San Francisco research team
Track and compile relevant press on short term rental regulations and legislation
Maintains a number of documents and internal processes relating to the ongoing legislative status and regulatory details to policy leads
Supports comprehensive tracking and reporting systems for each project, and , update and organize shared drives/files
Build relationships and working with cross-functional teams
Assist with other assignments and tasks as necessary
A bachelor's degree or from an accredited four-year institution
Exhibit strong process-oriented skills and strive to find the most efficient way to do things without sacrificing a high quality of work and/or results
Strong work ethic, and exhibit professionalism, courtesy and strong interpersonal skills
Ability to exercise judgment and maintain confidentiality
Demonstrate outstanding pro-active and multi-tasking abilities
Acute attention to detail and follow through, and are very organized
Ability to work effectively on multiple projects at once and meet deadlines
Excellent research, writing, and verbal communication skills related to public policy and legislation
Understanding of local city government structure and process

Research Coordinator Resume Examples & Samples

Graduate degree in economics, public policy, social work, or a closely-related field
Experience with navigating University of Washington and/or Washington State Institutional Review Board research procedures
Experience with using or analyzing administrative or complex longitudinal data
Social science research experience, particularly on politically salient issues related to labor market inequality such as the minimum wage
Mixed-method research interest or experience

Research Coordinator Resume Examples & Samples

Manage day-to-day operations of specific projects including logistics, scheduling, resource/equipment planning, staffing
Work with subject matter experts to enable process for improving and expanding conventions for analyst workflows
Manage collection of project-specific data
Own the logistics and reporting for these collections
Communicate directly with participants, tracking and responding to written requests and in-person as needed
Lead small to medium projects related to improving existing processes or launching new projects
Partner closely with Program Managers and team members on protocol/process development for existing and future collections
Continuously evaluate data collection tools and processes and offer solutions to ensure they are efficient, high quality, and scalable
Bachelor’s degree in a relevant field (including, but not limited to, Linguistics, Sociolinguistics, or Communications)
Excellent proficiency in US English and familiarity with language use specific to the United States culture
Detail-oriented, with experience balancing multiple tasks and deadlines
Ability to distill complex concepts into clear written guidelines
Experience working with various internal teams (including technical) to execute on requirements, surface and mitigate risks to delivery, and develop processes and tools
Experience with data collection, processing, throughput analysis & reporting
Excellent ability and methodology to troubleshoot and identify the root cause of issues
Dedicated, self-motivated and dependable
Willingness to support several projects at one time, and to accept reprioritization as necessary and to deliver high-quality work on schedule
Willingness to learn new processes and tasks in a growing and changing environment
Experience in understanding metrics and developing them, as required
Background in linguistics or experience with language processing, transcription, or annotation
Experience with Linux, query languages, and scripting languages

Research Coordinator Resume Examples & Samples

Creation of KTAZ, KHRR, KBLR & KDEN daily success stories and distribution of daily overnights
Assist in maintaining Arianna (overnight ratings program) and pull special trend reports as needed
Maintain Nielsen Enames module to ensure proper programming measurement
Create and design rating highlights sheets from both NSI and NSI-H during each sweep period
Assist in rating estimates for new programs for KTAZ, KHRR, KBLR & KDEN, along with analyzing competitive programming
Put together sales presentations and media kits as needed by staff
Help maintain and post information to the NBCU Portal
Assist Director on special research projects and analyses
Minimum one year TV research, media or agency experience
Willingness to travel, work overtime and on weekends with short notice as necessary
Must be willing to work at the station in Phoenix location
Must be 18 years or older
Must be covered by Solutions, NBCU’s Alternative Dispute Resolution Program
Demonstrated expertise using Microsoft Office applications including Excel, PowerPoint and Word
Bilingual preferred, but not required

Oncology Clinical Research Coordinator Resume Examples & Samples

Understands medical terminology
Demonstrates appropriate phone skills and effective use of the computer
Minimum two years of health care experience in ambulatory or acute care setting, Clinical Research experience preferred
Currently holds a Nebraska Medication Aide Registration if not a licensed medical provider or willing to acquire within one month of employment
Demonstrated knowledge of the clinical trial process and the Federal regulations that govern the conduct of clinical trials preferred

Research Coordinator Resume Examples & Samples

Processes research applications submitted to the hospital for review and approval
Reviews applications for completeness, contacts PI and/or study sponsors with hospital-related questions, works with PI and study coordinators to facilitate completed applications and review
Discusses/reports findings with Director of Revenue Analysis or Designee

Oncology Clinical Research Coordinator Resume Examples & Samples

Coordinates the initiation and activation of all new clinical trial protocols. This includes, but is not limited to, verifying Scientific Review Board (SRB), Institutional Review Board (IRB), Human Research Oversight Committee (HROC), data collection plans and finance/contract approvals prior to study activation. Coordinates the preparation of study tools including but not limited to study binders, medication diaries, eligibility checklists and flow sheets (as required)
Using Oncore®/Excel ®/Word, develops study tools, including but not limited to eligibility checklists, medication diaries, calendars, and flow sheets (as required)
In collaboration with the Research Nurse Clinician (RNC) and/or physician, reviews patients’ charts and medical history to confirm protocol eligibility and obtains source documents (i.e. medical record documentation) as needed. Under the direction of the RNC and/or physician, ensures that IRB approved informed consent form has been obtained, signed, placed in the medical record, and that a copy was provided to the patient
Registers consented research patients with study sponsor (e.g. industry, NCI Cooperative group, etc.) and inputs into Oncore® clinical trials database maintained by Cancer Institute of New Jersey
Maintains research record (e.g. patient consent, eligibility, Case Report Forms (CRF), registration confirmation, corresponding source documents, etc.) for all patients enrolled in Cancer Institute of New Jersey clinical trials. This includes, but is not limited to, Cancer Institute of New Jersey Network centers (Cancer Institute of New Jersey investigator-initiated trials), community physicians’ offices and hospitals
In collaboration with the RNC and physician, assists with grading adverse events using the most recent version of National Cancer Institute (NCI) common toxicity criteria or protocol specific grading scales. Completes Serious/Unexpected Adverse Event (SAE) form for all internal and multicenter serious/unexpected adverse events as required by study sponsors, federal requirements and institutional guidelines
Ensures research record (e.g. patient consent, eligibility, CRFs, registration confirmation, corresponding source documents, etc.) is maintained for all patients enrolled in Cancer Institute of New Jersey clinical trials. This includes, but is not limited to, Cancer Institute of New Jersey Network centers (Cancer Institute of New Jersey investigator initiated trials), community physicians’ offices and hospitals
Using Oncore®, provides regular reports to the tumor study group members and Principal Investigator on all studies to which he/she is assigned
Understands and anticipates needs of study sponsors. Serves as study liaison with study sponsors, schedules monitoring visits and conference calls. Provides accurate, timely, intelligent responses to sponsors’ queries
In collaboration with the RNC, assures that Cancer Institute of New Jersey personnel, including investigators, are conducting the study according to the treatment plan and GCP guidelines
Actively participates in weekly tumor study group meetings and conference calls (if applicable)
Actively participates in ongoing research specific quality assurance activities such as chart audits for protocol compliance
Communicates effectively with staff and outside agencies, and assists in the promotion of teamwork, contributes to OHRS espirit de corps
In collaboration with Tissue Analytical Services (TAS), ensures study specific deadlines are adhered to including the submission of pathology materials, serum, blood, urine and tissues samples, and CRFs
Collaborates with TAS and/or OCRC I/II staff members, to ensure procurement of protocol specific bio-specimens (e.g. blood, urine and tissue) are collected and processed according to protocol specific guidelines
Obtains and submits x-rays, pathology reports and any other specialized reports as needed
Maintains up-to-date knowledge and adheres to policies and procedures set forth by RBHS, Cancer Institute of New Jersey, FDA, and all regulatory bodies. Documents and maintains mandatory RBHS employee requirements such as Blood Borne Pathogens, Right-to-Know, Tuberculosis, Hand-Washing, as defined by Environmental & Occupational Health & Safety Services (EOHSS), Joint Commission on the Accreditation of Healthcare Organizations (JCAHO) and other institutional requirements

Research Coordinator Resume Examples & Samples

Relevant experience in clinical research with a strong cardiovascular knowledge base
Clinical cath lab experience preferred
Must have flexibility in hours based on needs of position including potential for off-hour need
Ability to effectively solve problems, balance multiple priorities and handle confidential issues
Thorough knowledge of federal and institutional policies governing clinical research required. Knowledge and experience of regulatory guidelines, FDA policies, and IRB guidelines a must
Proficiency with PCs and windows-based software, including Word and Excel, Microsoft Access

Clinical Research Coordinator, Senior Resume Examples & Samples

Bachelor’s degree in a field appropriate to the area of assignment AND four years of research administrative/coordinative program experience; OR, Master’s degree in field appropriate to area of assignment AND three years of research administrative/coordinative program experience; OR, eight years of progressively responsible research administrative/ coordinative program experience; OR, any equivalent combination of experience, training and/or education
Previous human subjects training (e.g. CITI certification) and four years experience as a research coordinator and/or research specialist senior conducting clinical research, and data analysis and reporting
Ability to follow strict protocols and standard operating procedures
Previous supervisory and training experience

Senior Clinical Research Coordinator Resume Examples & Samples

Serve as a resource to others for all aspects of conducting a complex and multi-site clinical study
Develop and implement plans and standard operating procedures under the guidance of study leadership
Collaborate effectively with others to ensure proper progress and completion of studies
Supervise activities of subordinates, if assigned
Train new staff in preparation and conduct of clinical trials
Provide oversight and guidance as needed to research staff
Collect and process specimens to meet study requirements, including saliva specimens and intravenous blood samples
Coordinate and participate in monitor visits, audits, and quality reviews (internal and external) in a professional manner
Prepare study staff and participate directly in recruitment/enrollment
Create and maintain a detailed tracking system for participants considered for enrollment. Track progress at regular intervals and report out to PI and study team
Proactively take initiative to ensure recruitment stays on track with the project timelines
Communicate study-related issues to investigators, sponsors, coordinating centers, study coordinators, clinical team, managers and other institutions in a timely fashion
Oversee data entry and validation to ensure accuracy, quality and compliance of data collection process
Ensure quality of data submitted from study sites and assure timely submission of data
Assist other members by educating, providing resources and consulting on difficult protocols or projects
Master’s degree in a field appropriate to the area of assignment AND three years related research experience; OR, Bachelor’s degree in a field appropriate to the area of assignment and four years related research experience; OR, Any equivalent combination of experience, training and/or education approved by Human Resources
Bilingual highly preferred (Spanish, Navajo/Diné Bazaad, other)
Previous supervisory experience

Research Coordinator Resume Examples & Samples

Bilingual (English/Spanish) preferred
Requires effective communication skills, both orally and in writing
Experience with computer spreadsheets and database management
Ability to understand and implement patient studies and protocols
Must have interpersonal skills necessary to coordinate research studies

Research Coordinator Resume Examples & Samples

Assists in developing research plans and project designs
Screens and schedules research participants
Coordinates protocol activities and works with research participants in accordance with human subjects requirements
Administers questionnaires and testing procedures
Collects, manages, and tabulates research data and ensures its accuracy and security
Assists in preparing project reports and manuscripts; processing regulatory documentation for submission
May also assist with coordination of some administrative duties, including keeping track of grant budgets and regulatory schedules; organizing meetings; and purchasing and replenishing of supplies

Research Coordinator Resume Examples & Samples

Analysis
Budget development and control
Organization

Senior Clinical Research Coordinator Resume Examples & Samples

Assist in planning and implementing the clinical study's goals and objectives; organize patient enrollment planning; conduct quality assurance activities, compile and analyze data
Develop and implement procedures, maintain records, track progress, and conduct quality assurance on data collected
Prepare, submit, and assist Director with multiple levels of research documentation (i.e. IRB submissions, educational materials, reports, grant renewal reports, and study forms)
Act as a liaison with medical staff, University Departments, ancillary departments and/or satellite facilities
Provide direct supervision to non-exempt staff (i.e. hiring/firing, performance evaluations, disciplinary actions, approve time off, etc.)
Maintain regulatory documentation
Perform related duties including level1 duties based on departmental need

Research Coordinator Resume Examples & Samples

Three years of grant management experience is required. Preference for that experience to have been in an academic environment
The ability to manage competing deadlines and be responsive to the needs of multiple PIs and departments
Demonstrable working knowledge of the OMB Uniform Guidance
Advanced experience with Excel

Senior Clinical Research Coordinator Resume Examples & Samples

Provide direct supervision to non-exempt staff (i.e. hiring/firing, performance evaluations, disciplinary
Bachelor’s degree in health-related field or equivalent experience
2-5 years relevant experience

Research Coordinator Resume Examples & Samples

Demonstrated ability to juggle and drive multiple responsibilities for self, peers, and superiors
Excellent writing skills and attention to detail
Excellent time management, interpersonal, and written and oral communication skills
Candidates must exercise good judgment and be able to work independently with minimal direction and as part of a team
Advanced skills managing databases (including Excel) and preparing charts/graphs from data
Experience with research methodology, interest in both qualitative and quantitative data. Following coursework is desired: corporate finance, managerial accounting, and business statistics
Strong technical skills, ability to efficiently use computer software and tools to complete analysis or communicate work. Facility and creativity with communication technologies
Positive attitude and strong interpersonal skills that enable working as an effective member on a small team
Commitment to CRPE’s mission and interest in the work of the Center
Experience with statistical software especially R, presenting data, and preparing reports
Experience working with fiscal and education data
Master's degree in a social science-related field
Coursework in corporate finance, managerial accounting, business statistics

Research Coordinator Resume Examples & Samples

Coordinates and assures integrity of all activities associated with conducting a clinical trial as it relates to compliance with local, state, and/or federal regulatory requirements
Assists Principal Investigators in the preparation and submission of clinical protocols, consent forms, and other documents to the scientific review committee, IRB and other regulatory organizations
Maintains regulatory files related to DVBIC clinical investigations
Communicates with research participants, staff, regulatory affairs and data management groups, laboratory and clinical investigators, management, and outside collaborators
Recruits, interviews, examines, counsels, and educates clinical trial volunteers, administer and obtain informed consent
May collect and analyze data to evaluate volunteer eligibility for enrollment
May collect, analyze and interpret laboratory and clinical data obtained during a medical evaluation, report significant values, findings, and events that require prompt attention to clinical investigators
Assists with the documentation and reporting of adverse events, completes and reviews Case Report Forms for patient eligibility, protocol compliance, omissions, errors, and submits these forms as required
Prepares and maintains written and electronic volunteer databases/logs
Perform data extraction and chart reviews of patients’ medical records
Reviews the source document file for information such as verification of critical variables, entrance criteria, visit date, and lab data
Ensures that research records are stored and secured properly, and that inventory and records are updated and properly maintained
Conducts data verification as indicated, documents, assists the investigator and protocol coordinator with questions, may transcribe and resolve queries of data in case report forms (hardcopy or electronic)
Prepares documents, under direction of project leads
Reports statistical analyses and descriptive data from patient's study books to be used in research reports

Clinical Research Coordinator, Senior Resume Examples & Samples

Eight (8) years equivalent combination of experience, training and/or education approved by Human Resources; OR
Bachelor’s degree in a field appropriate to the area of assignment and four years related research experience; OR,
Master’s degree in a field appropriate to the area of assignment AND three years related research experience

Research Coordinator Resume Examples & Samples

1-2 years of work experience, preferable in the broadcast media industry
Advanced skills utilizing Microsoft Excel and proficient in Microsoft Outlook Word, PowerPoint and Access
Dynamic, flexible, hard-working and highly organized
Superior interpersonal skills
Detail oriented with strong analytical and research skills
Familiar with Nielsen ratings, MRI, comScore & Media Math preferred

Research Coordinator Resume Examples & Samples

Conduct research literature searches and summarize findings in an organized format
Collect and manage survey data, download data from diabetes management devices, and complete electronic medical record reviews
Meet with families in busy outpatient and inpatient medical settings
Develop and maintain databases in Microsoft Excel and statistical software packages (SAS, SPSS, etc.)
Complete all required training modules related to the Responsible Conduct of Research (e.g., CITI Program training)
Evening and weekend telephone calls or meetings with study participants may be needed on occasion
Learning about type 1 diabetes by observing patient/family diabetes education classes and/or medical visits at the Texas Children’s Hospital (TCH) Diabetes Care Center, and completing readings and tutorials with the Principal Investigator and other diabetes experts at TCH
Learning to use the TCH electronic medical record, EPIC, to identify and track patients with diabetes
Learning how to recruit and enroll eligible families, and to obtain informed consent for behavioral research
Learning to collect and manage data from quantitative questionnaires, diabetes-related technologies such as blood glucose meters, and electronic medical records
Learning to complete required compliance-related documentation for behavioral research
Learning to develop an organizational system for managing all aspects of study implementation (e.g., participant incentives, study visit scheduling, medical chart reviews)
Learning to work independently and as part of a larger study team
Prior experience with Microsoft Excel and SPSS or SAS (statistical software programs) is required
Previous experience interacting with children and families and/or experience in health care settings is required
Experience with culturally diverse children and families is preferred
The individual is expected to be highly organized, keep detailed records, and display good verbal, communication, and problem-solving skills
Respectful, patient-centered interactions with participants, medical providers, and staff are expected at all times
Study activities will largely take place at three TCH/BCM locations in the Houston metro area: West Campus (Katy), The Woodlands, and Texas Medical Center. The candidate must be able to travel between those locations. Mileage for travel between locations and parking expenses will be reimbursed
Work is located in busy patient clinics, hospitals, office areas, and/or laboratories where there are potential exposures to blood borne pathogens (blood &/or other potentially infectious materials), drugs, chemicals, radiation, and physical hazards. Patient interaction and interaction with other employees is required

Research Coordinator Resume Examples & Samples

Organizes research protocols as designated by specific protocol guidelines
Conducts all testing procedures required by study protocol
Evaluates and analyzes clinical research data
Prepares documentation necessary to obtain initial and continued approval for the specific research protocol
Two years of relevant experience in a research setting with Bachelor degree or Six years of relevant experience in a research setting without a Bachelor degree

Research Coordinator Resume Examples & Samples

Oversees the organization and compliant execution of research projects with the proper allocation of resources and adherence to research protocol requirements
Oversees compliant research program operations and finances of assigned area(s)
Participates in process improvement activities
Potentially assists PI with research study design and development of research protocol
Supervises and coordinates research project budget development
Potentially negotiates industry-sponsored research budgets. Supervises research subject recruitment and data management
Minimum five years clinical research experience, including prior work lead and coaching experience
Advanced degree in health care, science or business may offset some of the experience requirement
Requires knowledge of budgeting, cost analysis, manpower planning, supervision and operational analysis
Demonstrates basic computer proficiency. Strong organizational, communication, interpersonal and analytical skills
Must be self-directed with demonstrated ability to work independently, yet establish cooperative relationships with colleagues

Research Coordinator Resume Examples & Samples

Bachelor's Degree in a related science or engineering field
Interest in, and knowledge of, energy-related technologies
Excellent written and verbal communication skills with the ability to convey scientific knowledge across technical and general populations
Excellent interpersonal skills, including the ability to interact with a diverse population comprising Princeton University community members, corporate executives, funding agency representatives, and external administrative staff
General knowledge of university research activities and sponsored research principles

Research Coordinator Resume Examples & Samples

Serves as primary study coordinator for research protocols in the outpatient clinic or at affiliated hospital as assigned by the Director
Directs the conduct of clinical studies to ensure adherence to the research protocol
Screens patient records, databases and physician referrals for identification of prospective candidates for research protocols
Interviews prospective subjects for participation in investigations and obtains informed consent
Participates in initiation visits/investigator meetings for assigned clinical trials (may involve travel) and implements these trials according to a deadline schedule mutually agreed upon by PI and sponsor
Educates human subjects for participation in investigations
Educates clinic/hospital personnel for participation in protocol conduct, data collection process and related issues as applicable
Ensures all study personnel have completed required training and training is documented, before conducting protocol related activities
Maintains consistent enrollment in protocols and provides monthly, written documentation of screening/enrollment/follow-up activities
Draws, processes,prepares and ships laboratory samples for clinical trials
Performs ECG’s, Holter monitoring and other procedures as directed by study protocol
Instructs Principal Investigator on procedures and tests that need to be performed in compliance with the study protocol and advises PI on the results of procedures and testing; calling to attention findings of clinical importance
Documents research related examinations, procedures, tests and other activities in appropriate clinic or hospital charts
Document phone conversations with sponsors, study subjects, physicians and coordinating organizations
Schedules follow-up visits for study subjects with appropriate personnel in and provides source documentation for activities conducted during these visits
Completes accurate and complete data entry into case report forms or pre-established computer programmed formats
Schedules and undergoes Coordinates and participates insponsor initiated monitor visits and quality assurance audits for periodic reviewing and querying of collected data in a timely manner
Identifies strategies to improve patient enrollment in research protocols in collaboration with the PI
Report all serious or unexpected adverse events immediately to physician or Research Director, maintains documentation and review of AE’s
Assist in reporting all serious or unexpected adverse events to appropriate regulatory agencies (sponsor, IRB) in a timely manner
Assists in maintenance of patient flow sheets and research data base
Acts in accordance with The Practices principles and practices
Performs delegated duties as assigned

Research Coordinator Resume Examples & Samples

Bachelor's Degree in a related field; four years of relevant work related experience in a research setting can be substituted in lieu of a degree
Experience using Electronic Medical Record Systems
Fully fluent in English and Spanish
Ability to tend to details
Ability to maintain confidentiality of patient information to include protected health information
Ability to communicate with patients in a compassionate, non- judgmental manner

Clinical Research Coordinator, Senior Resume Examples & Samples

Oversee the team of Clinical Research Nurses, Coordinators, and Cord Blood Collectors at CCBB staffed collection sites
Develop Team leads as mid-level managers
Coach, mentor and motivate team members
Perform all personnel actions, including interviewing, hiring, and performance management
Develop and strengthen current communication channels to allow for sharing of best practices across sites
Visit collection sites regularly
Ensure that scheduling coverage for collections at all hospital sites is complete for each month
Set goals for collection sites
With the assistance of the Marketing Manager, the Education Specialist and the Collection Sites Team Leads, develop and implement incentive programs to increase the number of banked cord blood units and to increase participation of hospital medical staff
Identify and share best practices across sites
In conjunction with Marketing Manager, Education Specialist and Collection Sites Team Leads, develop and oversee implementation of continuous improvement strategies for staffed, hybrid and kit sites
Work closely with the Marketing Manager and the Education Specialist to develop programs with the goal of promoting the Carolinas Cord Blood Bank and to develop education tools that promote public awareness of cord blood banking the community
Present to community groups as needed to increase awareness of cord blood banking
Represent the Medical Director in interactions with hospital staff, on national and international cord blood collection committees, and at outside meetings and conferences
Maintain liaison with hosting hospital managers and staff to solve operating problems that may arise at any one of CCBB's collection sites
Ensure good relationships with staff at CCBB's hybrid sites is maintained and strengthened
Work closely with CCBB Marketing Manager to provide regular updates to hospital staff and collection overview for directors, doctors and staff from affiliated sites and to develop educational tools that promote public awareness of cord blood banking in the community
Collaborate with Collections Logistics Manager on the development and modification of standard operating procedures (SOPs) related to collection of cord blood
Work closely with QSU staff, the Collection Logistics Manager and the Training Coordinator to prepare training materials for new and updated operating procedures
Represent collections at outside and internal audits including FACT, FDA and QSU
Completion of an Associates degree plus a minimum of six years of research experience, or
Completion of a Master's degree and a minimum of 2 years of research experience

Senior Clinical Research Coordinator Resume Examples & Samples

Helping with patient enrollement and patient interaction
Working with site budgets
Ensuring regulatory documents are in place
Responsble for managing any new CRC hires
Management over 3 clinical staff

Research Coordinator Resume Examples & Samples

Serve as the Executive Assistant to the Executive Vice President, Research: plan meetings, route phone calls, edit power points, and manage calendars
Track and ensure delivery of acquisition scripts and screeners; distribute materials and assignment information to contractors and staff
Research and write due diligence reports for National Geographic Partners
Write quick passes for acquisitions
Quality Check shows which have completed research process
Track contractor expenses and payments, and process invoices
Consistent maintenance of department project database (FILEMAKER) including support for remote users
At least 1 year of research experience in an academic or professional context
Proficient in Microsoft Office. Experience in FILEMAKER and VPS is a plus
Proficient is Spanish is a plus

Lead Clinical Research Coordinator Resume Examples & Samples

Train new and current Clinical Research Coordinators and Research Assistants to ensure effective coordination of training activities in the clinical trials processes
Assist CRC’s and RA’s with assigned tasks as necessary
Provide clinical support and assistance in the assignment of CRC’s, Raters, and other staff
Troubleshoot and resolve clinic, protocol, and SOP issues and advise CRC’s
Assist coordinators with assigned tasks as necessary
Problem solve protocol issues with staff as necessary
Work closely with the Research Manager to improve and streamline clinic processes
Assist the Research Manager with projects and tasks as assigned
Fill in as needed in the absence of CRC’s
Acting Supervisor or point of contact in the absence of the Research Manager
Resolve problems quickly + in a positive manner
Minimum of 2 years of clinical research experience required; CCRC strongly preferred

Research Coordinator Resume Examples & Samples

Collaborates with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols
Assists with the recruitment, selection and monitoring of research project participants
Manages the handling of adverse events, compliance and other participant-related issues
Minimum two years prior clinical research or health care experience required
Bachelor's Degree in a health care or science field can substitute for years experience

Senior Clinical Research Coordinator Resume Examples & Samples

Data entry for clinical research projects including but not limited to
Entry of clinical data from test requisition forms
Entry of clinical data from medical record forms
Entry of clinical data from phone interview
Email/Phone follow-up for research projects as directed by supervisor or supervisor’s designee
Data queries development and execution as needed
Data analysis as directed by supervisor or supervisor’s designee
Literature review related current and active research projects
Other tasks to assist with current research, variant assessment/reporting or marketing group projects as directed by supervisor or supervisor’s designee
Occasional coverage for clinical assistants as needed

Research Coordinator Resume Examples & Samples

3 years working with American Indian communities
2 years of experience as a Project Coordinator or similar
5 years working with American Indian communities

Senior Research Coordinator Resume Examples & Samples

Coordinates and ensures accurate protocol implementation and conduct for all assigned protocols
Coordinates regulatory and IRB interactions in collaboration with the ICTR regulatory staff. ? Recruits, screens, and enrolls research participants
Assists Principal Investigator with informed consent
Coordinates care for research participants enrolled on assigned protocols to ensure that the study is implemented as it is written and that all required data are available and collected
May collect, process and ship laboratory specimens
Performs patient/family education about clinical trials as well as the research protocols
Ensures research needs are met at all family meetings (discuss progress of treatment, changes in therapy)
Acts as liaison between patient and physician concerning problems, adverse reactions, and other patient care issues, that may be related to the study. Follows-up with patients during each clinic visit to answer questions and assess for toxicities
Coordinates affiliate involvement with study conduct, Investigational Pharmacy, Research Office, Diagnostics, Credentialing, etc., as needed
Five years of relevant experience in a research setting with a Bachelor's degree or nine years of relevant experience in a research setting without a Bachelor's degree

100

Senior Clinical Research Coordinator Resume Examples & Samples

Provide oversight for the preparation, review, submission and maintenance of regulatory activities/submissions within our team to the national IRB; ensure accuracy and timeliness of distributing regulatory updates to all collaborative parties
Bachelor’s degree in a field appropriate to the area of assignment and four years related research experience; OR, Master’s degree in a field appropriate to the area of assignment AND three years related research experience; OR, Any equivalent combination of experience, training and/or education approved by Human Resources
Bilingual (Spanish, Navajo/Diné Bazaad, other)

101

Senior Research Coordinator Resume Examples & Samples

Manage qualitative workflows and pipelines from across the network
Work with internal and external departments to understand research objectives
Develop and program recruitment screener to target specific audience groups per client need, for applicable qualitative projects
For applicable qualitative projects, develop facilitation guides and/or community engagement tasks
Oversee and manage vendors for execution of online work as well as moderate members of community sites to ensure quality research feedback
Manage scheduling and booking of focus group facilities, online platform vendors and respondent incentives
Assist with the development of analysis in various formats such as tab plans, graphs, memos, written report summaries, and/or efficient visual ways of understanding the data
Weekend and non-traditional business hours maybe required for this very fast paced role
Minimum of 3 years proven research experience, with at least 2 years in Qualitative research
Experience with both in-person and online moderation
Must have an understanding of general research processes and research design of qualitative research techniques
Solid grasp of traditional media research tools and social media platforms

102

UX Research Coordinator Resume Examples & Samples

Manage research projects across a variety of methodologies
Conduct qualitative studies (usability studies, click-tests, etc.), analyze data, share findings
Field surveys, analyze responses, and report findings
Maintain ongoing research initiatives including projects with external research vendors
Work cross-functionally with design, product marketing, and product management

103

Research Coordinator Resume Examples & Samples

Work with research consultants to identify and screen candidates, communicate with internal relationship representatives, manage and track approvals, outreach to participants, and coordinate scheduling
Establish user criteria and develop SQL statements to pull data from various databases
Partner and coordinate with individuals who have access to customers
Maintain participant lists for multiple studies
Build a database of participants that is continuously maintained and updated
Establish innovative and efficient ways to attract participants that comply with internal regulations regarding customer contact and communication
Screen participants for usability tests by interviewing participants over the phone and distributing/managing questionnaires. Manage, track, distribute and store participation incentives, NDA's and thank you gifts
Logistics such as schedule sessions, maintain calendars, schedule conference rooms, confirm with participants and other tasks for both remote and field research
Proactively communicate status updates and changes that impact ongoing research
Maintain and update SharePoint User Experience Research site - includes keeping Research Library up to date with all final reports, maintaining upcoming research calendar, ensuring that UxR marketing content is current
Manage research booth at Global Payment Conferences
Exemplary business communication and networking capabilities; ability to assess project issues early, and communicate appropriately to help manage expectations
Project management: ability to "juggle" time and effort across multiple projects and proven ability to deliver results within a specified time
Creative problem solving skills - filling research quotas is like putting together a puzzle and the successful coordinator will be someone who likes to work on a problem until it is solved
Exemplary organizational skills and penchant for developing and following efficient processes
Ability to organize and maintain accurate and timely records of contacts, activities, and schedules
Experience with Microsoft Project, Excel, and PowerPoint
Basic knowledge of SQL
Ability to travel regularly
Microsoft SharePoint work and site management
Microsoft Live Meeting

104

Research Coordinator Resume Examples & Samples

Experience in an academic medical center
Experience as a research study coordinator
Experience in cardiology clinical research
Familiarity with interpreting regulatory and contractual documents, identifying and resolving ambiguities, negotiating pricing and payment terms, and interpreting complex implications of research protocols
Knowledge of the Medicare Clinical Trials Policy and other federal, state and institutional clinical research regulations
Experience with using International Classification of Diseases, 9th Revision (ICD-9), Current Procedural Terminology (CPT), and Healthcare Common Procedure Coding System (HCPCS) billing codes in a clinical research environment
Strong working knowledge Microsoft Office Suite

105

Assistant Clinical Research Coordinator Resume Examples & Samples

Bachelor's degree in Psychology, Epidemiology, Public Health, Neuroscience, or Human Biology
Prior experience working with human subjects
Prior experience in behavioral sleep medicine

106

Research Coordinator Resume Examples & Samples

Prior experience in clinical or laboratory research in an oncology setting,
Knowledge of FDA and NIH requirements relating to research involving human subject
Experience in clinical trial development, implementation and analysis,
Experience with Microsoft Office, experience with case report forms (ideally paper and electronic)
Oncology clinical trial coordination experience
Knowledge of University of Washington/Fred Hutchinson Cancer Research Center/Seattle Cancer Care Alliance processes

107

Research Coordinator Resume Examples & Samples

Master’s degree in psychology, social work or counseling
Experience facilitating therapeutic interventions with groups
Experience working with high-risk mothers and children

108

Assistant Clinical Research Coordinator Resume Examples & Samples

Prior experience or exposure to conducting psychotherapy
Prior research experience including human subject interaction
Prior experience or exposure to behavioral sleep medicine

109

Assistant Clinical Research Coordinator Resume Examples & Samples

Demonstrated success with building partnerships with community agencies
Proficiency with Microsoft Office, ACT!, and REDcap
Skilled in effective risk management
Trained and skilled in motivational interviewing and stage-tailored interventions
Knowledgeable of nicotine addiction and its treatment

110

Assistant Clinical Research Coordinator Resume Examples & Samples

BA/BS in health sciences, physiology, biology; coursework or equivalent in behavioral health, gerontology, or related fields
Attention to detail and strong organizational and time management skills
Good interpersonal and communication skills are essential (both oral and written)
An excellent telephone manner and excellent verbal English communication skills
Experience with telephone and or in-person interviews in a research setting
Experience working with older adults and sensitivity to health issues and other issues of ageing
Experience with human subjects research, data collection and scientific procedures
Good computer skills, particularly with FileMaker, Excel and Word

111

Research Coordinator Resume Examples & Samples

A degree and/or prior work experience in chemistry or a related field
The ideal candidate will be a creative, enthusiastic self-starter who can react to the changing needs of the organization and take the initiative to bring to the attention of the PIs ideas, suggestions or solutions that better meet the goals of the unit
Excellent time-management and organizational skills and the ability to independently manage work priorities across multiple complex projects, meeting stringent timelines
Self-motivation and the ability to maintain a vision of overall program goals while managing and performing specific tasks with precision, accuracy, and meticulous attention to detail in an intense work environment
Strong collaborative skills for work with large, diverse groups, strong interpersonal skills, excellent written and oral communication
Experience with standard office software, reference management tools, email, financial modeling and budget preparation in Excel
Experience and aptitude with Mac- and Windows-based computing, and the ability to switch freely for cross-platform use
Experience with scientific manuscript preparation and editing

112

Research Coordinator Resume Examples & Samples

Assist in developing research plans and project designs; screening and scheduling research participants
Coordinating protocol activities and working with research participants in accordance with human subjects requirements
Administering questionnaires and testing procedures
Collecting, managing, and tabulating research data and ensuring its accuracy and security
Assist in preparing project reports and manuscripts; processing regulatory documentation for submission
Strong knowledge and understanding of the operational, logistic, and administrative requirements of research studies; ability to establish and maintain efficient work flow and administrative processes
Excellent organizational skills and attention to detail; skill in organizing resources and establishing priorities; ability to manage multiple tasks and complete them on time
Excellent interpersonal and communication skills; ability to interact with a diverse population of program participants
Demonstrated computer skills and proficiency with MS Office
Knowledge and experience with computer spreadsheets and database software
Strong written communication skills; ability to document project plans and activities, draft reports, and maintain project correspondence

113

Research Coordinator Resume Examples & Samples

Computer-based statistical software usage and the interpretation of findings in applied research settings
Conducts basic statistical analyses in database software, creates graphs and tables in spreadsheet software, and writes/edits in word processing software; prepares statistical and database reports, tables, graphs, narratives and questionnaires in print, electronic and web-enabled formats
Clearly and accurately communicate orally and in writing, complex and/or technical information
Proficiency in using computer databases, spreadsheets and word processing software
Excellent oral and written communication skills, critical thinking abilities and organizational skills
Knowledge of federal policy for the protection of human research subjects and other applicable regulations and standards
Proficiency in reviewing federal and private sponsors for grant opportunities and writing grant applications

114

Research Coordinator Resume Examples & Samples

Provide administrative support for meetings and training, as needed, including room set-up, materials, refreshments/meals and logistics
Assist with setting up departmental meetings
Coordinate travel requests (may include booking flights, hotel and ground accommodations)
Create, submit and manage expense reports
Provide data entry and project support to departments as assigned
Process various forms related to documenting activities of functional areas
Provide administrative support for clinical and technology grant programs
Tracks internal and external contracts, protocols, and legal agreements, such as with consultants, research partners, and ethics committees
Facilitates vendor relationships and assists with purchasing and order tracking
Process purchase orders, payments
Mailing of packages
Order and maintain office supplies
Assist in ad-hoc projects or other duties as needed. Additional assignments may be found in various functional areas
Minimum 5 years of experience supporting engineering teams or equivalent. Medical device or grant experience preferred. Experience within a research organization is a plus
Excellent communication (written, verbal), presentation and documentation skills
Comfortable with managing multiple projects simultaneously, with ability to switch focus between projects quickly

115

Research Coordinator Resume Examples & Samples

Maintains clear communication with customers regarding mutual expectations
May have physical requirement to lift no more that 10 lbs
May handle/work with biohazards
Training may be required for phlebotomy and EKG's/ECG's prior to performing on study participants

116

Research Coordinator Resume Examples & Samples

Data entry
Conduct data quality assurance checks
Clean research data Run queries / reports to fulfill data requests Interview research subjects
Perform literature searches and prepare literature reviews
Conduct patient interviews

117

Research Coordinator Resume Examples & Samples

Participate in data collection, management, and coordination and execution of study activities
Maintain excellence in research protocol adherence
Assist with regulatory compliance
Prepare and submit regulatory reports and reports to collaborators, and other parties as needed
Participate in study promotion, advertising, and outreach
Recruit study participants and manage their study participation
Assist with data analysis, writing results, and presentations for broad communication of study findings
Assist with writing, editing and reviewing of abstracts, reports and scientific articles for submission to conferences and publications
Develop PowerPoint or similar presentation tools appropriate to report research results to state and or national audiences
Sound analytical and organizational skills
Excellent interpersonal skills and ability to work collaboratively as part of a team
Ability to identify potential problems and trouble-shoot solutions
Proficiency in scientific/ research writing
Demonstrated application of specific research methods for clinical research, patient recruitment, and the management and conduct of research studies in diverse settings
Experience with research quality monitoring is preferred
Experience in communication (written and spoken) with medical providers, researchers, quality improvement teams, and patients is preferred
Experience with institutional review board (IRB) applications and renewals is preferred
Proficiency with REDCap database software is preferred

118

Clinical Research Coordinator, Senior Resume Examples & Samples

Ethical and participant safety considerations. Provide division or department-wide training in ethical conduct of research. Serve as expert resource to study teams as they design studies, so they include specific safeguards to ensure ethical conduct and protect vulnerable populations. Articulate the reasoning for an individual protocol's inclusion and exclusion criteria. Serve as a resource to help staff and patients recognize the difference between clinical care and clinical management of research participants. Independently develop documents related to safety and security. Serve as an expert resource for development and implementation of RDSPs, DSMPs, and Conflict of Interest plans across multiple studies or study teams
Data management and informatics. Use and train others in Electronic Data Capture (EDC) systems, technologies, and software necessary for study operations. Independently design CRFs to collect data according to protocol. Select methods of data capture and implement at the unit level. Investigate incomplete, inaccurate, or missing data/documents to ensure accuracy and completeness of data. Oversee the creation and use of queries, summaries, and reports. Develop system/framework for QA processes for multiple studies or for entire unit. Develop quality assurance systems for research data; ensure that QA SOPs are updated and followed by study teams. Implement quality assurance systems across multiple studies, or across entire unit, department or division. Recognize and report vulnerabilities related to security of physical and electronic data; recommend and lead implementation of processes, policies, and systems to ensure data security and data provenance
Scientific concepts and research design.Train others in the basic concepts of study design. Conduct and synthesize literature reviews, and independently develop proposals or protocols. Assess and determine solutions for operational shortcomings of proposals and protocols. Identify and collaborate with various stakeholders to ensure adequate design, implementation, and testing of study aims
Leadership and professionalism.Assist research colleagues in identifying efficiencies and improving process. May provide significant contribution and influence upon research work, activities, or productivity of project teams or across multiple groups. Network and encourage leadership opportunities for staff within a small work group. Lead a committee or task force. Actively seek out continuing education opportunities for self and study team members. Serve as a unit-wide expert resource for issues related to professional guidelines and code of ethics. Identify potential problems and risks to the participant, study, and institution. Maintain Duke and project specific training requirements. Develop solutions to proactively ensure unit,department, or division compliance with training requirements. Create strategies that enhance cultural diversity and cultural competency in the design and conduct of clinical research
Study and site management. Provide expert guidance to study team members to ensure participant care expenses have been set up correctly and that financial charges/expensed route in a timely manner; troubleshoot, escalate, and resolve issues. Collaborate with the financial analyst to establish financial monitoring systems. Coordinate with financial teams, PRMO, etc. Determine when financial reports are not working as planned and collaborate with sponsor and financial managers to troubleshoot. Develop study budgets. Coordinate operational plans for multiple research studies. Develop systems and documents including processflows, training manuals, and SOPs to be used unit, department, or division-wide. Work with sponsors/study teams to arrange required training. Lead site initiation, monitoring, and closeout visits and activities; provide feedback to the study team members. Develop and implement closeout procedures for multiple studies, unit, department, or division. Inform investigators and oversight organization regarding appropriate feasibility, recruitment, and retention strategies. Determine and implement alternative solutions to accomplish recruitment and retention milestones. Use system reports to ensure unit, division, or department compliance with institutional requirements and other policies; assist team members with understanding these requirements and policies. Oversee study teams# maintenance of Delegation of Authority Logs and training of KP on study specific duties
Communication and team science. Lead team meetings. Include others in decision-making, and escalate issues appropriately. Communicate with sponsors, subcontractors, or vendors and take action when communication has stalled. Act as an expert resource to junior staff liaising with sponsors, subcontractors, or vendors. Maintain training requirements. Develop solutions to proactively ensure study team members' compliance with training requirements. Evaluate the need for cultural diversity and cultural competency in the design and conduct of clinical research. Make recommendations to investigative team

119

Research Coordinator Resume Examples & Samples

Bilingual in Spanish
Phlebotomy trained
Current Baylor employees eligible to transfer are encouraged to apply

120

Research Coordinator Resume Examples & Samples

Work with subject matter experts to enable process for creating, improving, and expanding conventions for analyst workflows
Communicate directly with data analysts to improve and operationalize projects
Partner closely with Data Specialists and team members on protocol/process development for existing and future collections
Continuously evaluate data processing tools and processes and offer solutions to ensure they are efficient, high quality, and scalable
Experience with data processing, throughput analysis & reporting

121

Research Coordinator Resume Examples & Samples

Well developed research skills including experience developing questionnaires
Strong computer knowledge and experience with MS Office (Excel, Word, PowerPoint, Access), Outlook, and Photo Shop
Working knowledge of HTML coding and SPSS would be considered an asset
Demonstrated ability to review and identify trends and anomalies in data
Experience coordinating research projects independently
Ability to speak French is an asset
1-2 years of market research experience, ideally in a retail environment

122

Assistant Clinical Research Coordinator Resume Examples & Samples

At least one year of relevant experience or an equivalent combination of experience, education, and training
Experience with maintenance of clinical study binders and with interface with electronic record-keeping methodologies
Familiarity with clinical registries/databases

123

Lead Clinical Research Coordinator Resume Examples & Samples

Ensures that protocol and subject milestones are entered and updated in timely manner in medical record and clinical trial management systems
Develops criteria for enrollment of prospective study subjects based on goals and objectives of project
Verify screening procedures are performed within protocol specific window
Assists in obtaining informed consent in accordance with applicable federal regulations and University policies

124

Research Coordinator Resume Examples & Samples

Proficient knowledge of SPSS (and/or R) and Microsoft Office Suite (especially Excel). Experience with E-Prime and FileMaker Pro, or the willingness to learn these applications
Experience with various stages of grant-funded research, including: preparation of grant applications, designing studies that fall within the scope of a project proposal, managing budgets, and reporting results to funding bodies
Careful attention to detail and an ability to anticipate future problems
Ability to create and maintain web pages and other multi-media projects
Data analysis skills
Comfort working with all age groups

125

Research Coordinator Resume Examples & Samples

Consult with research leadership to determine scope and extent of testing and analysis requirements
Determine equipment and materials needed to support testing and analysis efforts;, acquire materials as required
Oversee and coordinate set up and conducting of testing processes as previously determined
Analyze and document results of testing processes
Oversee or conduct calibration and maintenance of testing equipment; maintain required inventories of materials and supplies needed in testing process
Conduct ongoing review of testing methods and procedures; implement modifications to existing methods or develop new ones to improve process
May provide work direction and guidance to student assistants and other research support personnel
Education:High School Diploma, Technical Diploma, Associate's degree and/or two years of college level course work or an equivalent combination of education and experience
Work Experience:Six years of job related experience
Skills:Application of advanced laboratory testing processes and procedures specific to assigned specialty; analysis and documentation techniques, report writing, presentation and communications; work direction
Preferred Education:Bachelor's degree (BA/BS)

126

Research Coordinator Resume Examples & Samples

Previous experience in clinical trials required
Bachelor's degree or equivalent work experience in a healthcare related field required
Must be eligible and attain the status of Certified Clinical Research Professional (CCRP) or
Ability to work with and communicate to a diverse work force at all levels of the organization
Strong communication and leadership skills required
Must be able to adapt easily to change and lead others in a team environment
Strong computer and organizational skills
Understanding of ethical principles, culture and values of medical research, including Good
Minimum of three (3) years direct research experience as a Research Coordinator or similar

127

Research Coordinator Resume Examples & Samples

Master’s degree in Life Sciences or related
One year experience in research project management in the science or technology environment
In lieu of a degree, consideration will be given to an equivalent combination of related education and required work experience.　
Excellent written and oral communication skills with the ability to express ideas clearly and effectively
Familiarity with scientific and technical language
Strong organizational and time management skills; must have the ability to exercise sounds judgment in prioritizing tasks
Self-motivated and proven ability to work independently
Must be creative, thorough, and able to balance multiple tasks and handle confidential information with discretion
Ability to perform background research for specific grant programs, develop knowledge of federal and other granting programs, establish timelines and best practices for proposals, and function as an integral member of the proposal development team
Excellent interpersonal skills with the ability to represent PVM in a professional manner in interactions with internal and external stakeholders

128

Research Coordinator Resume Examples & Samples

Becomes familiar with all protocols assigned, as well as has a basic knowledge of all studies being conducted for Midwest Physician Administrative Services. For assigned studies, initiates study start-up activities including study initiation meeting, scheduling subject visits, along with scheduling any outside personnel or tests for these visits
Responsible for initiating and maintaining appropriate regulatory documentation and for facilitating all interaction between investigative site, sponsor and IRB
Evaluates volunteer subjects for potential study qualification in accordance with inclusion/exclusion criteria provided by study sponsor. Assists in subject recruitment
For qualified participants, initiates medical and social histories, physical exam, and physiological measures as indicated in protocol. Records this data in detail. Schedules study visits as required by protocols
Ensures appropriate laboratory, x-ray and other diagnostic examinations are scheduled and completed per study protocol. Oversees any outside services as required
Reviews medical, laboratory, and other diagnostic data on study patients. Notifies principal investigator of any abnormal values or any significant changes in these values. Notifies and follows up with subjects as required
Reports serious adverse events to principal investigator, sponsor and IRB (if required) in a timely manner. Follows up with subjects or subject's family members in accordance with procedures
Collects data requested by protocol. Ensures accuracy of data obtained. Collates and enters data into research charts, sponsor case report forms, and/or remote data entry equipment in a timely and precise manner
Ensures that all study drug/devices received is accurately documented and stored in locked location. Ensures that study drug/devices are maintained in appropriate temperature controlled environment. Verifies that all study drug/devices are correctly labeled, and packaged. Ensures that appropriate study drug/devices are dispensed to patient along with detailed instructions on use. Maintains accurate documentation of each of these along with return of test article
When studies require other supplies and/or equipment, coordinator will ensure their availability and ensure proper orientation has occurred prior to use
Ensures subject compliance with study treatment and study visits. Notifies sponsor of any deviations from protocol. Whenever possible, obtains permission prior to deviation, i.e., protocol exceptions
Schedules routine study reviews with sponsor monitors or appointed sponsor representative. Arranges access to all subject records for the indicated time period of review. Allows time to respond to monitor questions and to make correction to case report forms. Promptly responds to sponsor queries
Prepares for and completes close out procedures for terminated studies. Ensures all FDA, sponsor, and center regulations have been followed
Assist with training of other center personnel as directed
Works with other research coordinators and research assistants to provide back-up replacement during absences, and follow-up as needed
Provides health practices information and education to practice and study subjects regarding medications, diseases, diet, exercise, and any special procedures. Assists subjects by providing appropriate referrals to physicians, clinics, or agencies
May provide on-call service for study subjects during evenings and weekends on rotation basis with other research staff
Acts as a liaison for subject/physician telephone calls
Actively participates in clinical meetings, rounds, and departmental meetings
Participates in supervision and evaluation of research assistants
Participates in other center activities such as special projects, and any other duties as assigned by Director
Must take the certification test within 3 years of date of hire
Excellent clinical assessment skills
Detail-oriented and highly organized
Ability to understand technical research protocol
Able to make decisions independently and yet must be team oriented
Must possess ability to articulate and clearly communicate study information to patients, and other health care processionals
Professional demeanor with ability to interact with pharmaceutical/sponsor representatives, regulatory agents, medical center administration, medical staff, peers, and patients
At least one year of research experience as a clinical research coordinator is recommended

129

Research Coordinator Resume Examples & Samples

Conducting psychosocial intervention with parents across multiple time points
Organizing essential materials and measures to be given to families
Determining eligibility and recruiting research participants
Interfacing and communicating with medical providers
Collecting research data (both paper and electronic-based)
Scheduling follow-up visits with participants

130

Research Coordinator Resume Examples & Samples

Acquiring, managing, analyzing and archiving data
Geographic analysis
Meeting planning
Abstract, manuscript and grant editing

131

Research Coordinator Resume Examples & Samples

Recruit, screen, educate, and assist potential study enrollees and their families throughout the length of the study
Schedule research subjects’ appointments for tests and procedures
Responsibly handle and ship biospecimens
Retrieve and submit test results to appropriate party or data coordinating center
Enter study data from patients, families and medical records into a computerized database and/or on a case report form
Regulatory work including drafting, submitting, and amending new or ongoing research protocols for Institutional Review Board review
Ensure compliance with NIH and IRB regulations
Maintain records and regulatory documents
Work effectively with a team of research coordinator to ensure appropriate and high-quality cross-coverage of different protocols
Participate in weekly project meetings
Help meet study timelines as determined by the PI
Preferable to have experience using EPIC database for patient care records

132

Assistant Clinical Research Coordinator Resume Examples & Samples

Four year college degree in a related field
Experience working with healthcare professionals and clinical research participants
Experience with University related research policies and procedures

133

Research Coordinator Resume Examples & Samples

Requires skills in communicating, recruiting and data collection (qualitative and quantitative)
Knowledge in conducting heights, weights, GPS and CSA measurements, behavioral, and physical activity questionnaires
Skill and comfort with using PC computers including Word, Excel, Access, PowerPoint, and Survey Monkey (or equivalent) software programs

134

Trauma Research Coordinator Resume Examples & Samples

Develop and implement data collection processes related to specific research protocols
Responsible for managing database and performing data analysis
Assist with the preparation of Institutional Review Board (IRB) applications and reports for Annual Continuing Reviews
Plan and participate in research and performance improvement studies
Perform literature searches relevant to clinical research topics and references for bibliographies
Assist with the preparation of electronic presentation media for national meetings/conferences
Assist with the preparation of abstracts for national conferences
Compile, prepare, and review manuscripts for publication; consult with medical director regarding arrangements and compilation of content; proofread copyedited materials as required
Participate in clinical research initiatives
Coordinate and supervise activities with Clinical Research Organizations (CRO) that represent sponsored clinical trials
Works within defined protocols and current HIPPA regulations

135

Senior Clinical Research Coordinator Resume Examples & Samples

Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of data queries
Prepare and or complete regulatory related reports and IRB submissions. Maintain and organize study regulatory binders, enter all required study data on an ongoing basis
Ensure all study related samples are collected, properly prepared and shipped according to the protocol requirements and IATA/DOT regulations
Responsible for organizing and preparing for both internal and external auditing and study monitoring visits
May be responsible for tissue sample work
Provides day-to-day work direction to CRC I and II. Assists Clinical Research Managers with completion of performance reviews and provides input as needed for development and corrective action activities
Contributes to the development of research protocols and understands research design
Bachelor's Degree required and at least 3-5 years of equivalent experience required. Experience working in a medical or scientific research setting or comparable technology orientated business environment preferred. Performs primary duties with independence and has progressed to mentoring junior staff
Excellent organization and communications skills required. Strong interpersonal skills - ability to effectively interact with all levels of staff and externals contacts
Must be detail oriented and have the ability to follow-through. Ability to effectively manage time and prioritize workload
Must practice discretion and adhere to hospital confidentiality guidelines at all times
Must have computer skills including the use of Microsoft Office
Ability to coordinate PI initiated multi-center studies

136

Research Coordinator Resume Examples & Samples

Passion for customer empathy, people, and research
2‐3 years’ experience in some form of recruiting, project coordination, or administrative support in a software or technology company
Ability to work in a fast‐paced, frequently changing environment while providing a superior level of support
Solid project management, organizational, and multi‐tasking skills. Must be proactive, take ownership, respond quickly, and have an unparalleled eye for detail
Proficient in Google Docs, Outlook and Excel
Experience managing relationships with multiple internal teams
Ability to solve problems creatively, proactively identify issues and inefficiencies, and provide resourceful solutions
Basic familiarity and interest in user research techniques a definite plus!
Effectively identify, recruit, and schedule participants for research studies
Handle all scheduling, coordination, and communication between the research team and research participants
Manage User Participation Agreements and track process
Create and manage screening surveys (Survey Monkey and Ethnio)
Manage participant incentives, including handling, purchasing, tracking, and accounting
Manage multiple participant databases
Conduct background research on participants and create participant profiles
Perform other tasks and support the team in projects aimed at maintaining and improving the research and participant recruiting program
Manage vendor relationships, such as third party research panel providers and rental facilities

137

Assistant Clinical Research Coordinator Resume Examples & Samples

Verbal and/or written fluency in Spanish or Mandarin is required
Strong interpersonal skills, sensitive to a range of participant needs
Previous experience with clinical research desired
Proficiency with REDCap and computer data entry
Excellent organizational skills and meticulous with record keeping

138

Research Coordinator Resume Examples & Samples

Gather and analyze data
Assist in the development of policies and procedures
Coordinate the development of research project reports
Review and analyze relative literature
Assist with modification of protocols
Consult with other units and community agencies concerning research project
Assign work; ensure proper workflow of the unit; act as lead worker
Serve on departmental and/or university committees as requested or required
May provide supervision to student employees and research assistants
Performs related duties based on departmental need

139

Research Coordinator Resume Examples & Samples

Demonstrated ability to complete detailed assignments in a timely and accurate manner
Demonstrated verbal, written, and interpersonal communications skills
Demonstrated customer service orientation that allows for effective interaction with study participants, patients, students, faculty and staff
Demonstrated ability to work with and adapt to new technology
Demonstrated ability to use MS Office at an advanced level, particularly Excel and its data analysis ToolPak, Word and PowerPoint

140

Research Coordinator Resume Examples & Samples

Coordinate participant recruitment, enrollment, and follow-up
Assist in development and implementation of recruitment strategies
Monitor data collection, cleaning and analysis
Act as liaison between subject coordinators and investigators
Coordinate meetings of project personnel
Responsible for incentive payment process
Responsible for processing IRBs and IRB compliance
A bachelor’s degree in a health related field is required; a master’s degree in Public Health is preferred
A minimum of three (3) year’s work experience in a clinical research related field is required
Candidate must have excellent communication skills, attention to detail, strong interpersonal skills, and organizational skills
Excellent computer skills, including expert knowledge of Microsoft Office products including Word, Excel, Outlook, Access and PowerPoint
Previous experience providing CTR/HIV counseling and testing
Candidate should have experience working with the LGBT community
Experience with online recruitment of research participants

141

Research Coordinator Resume Examples & Samples

Develops in-depth understanding of each study protocol to ensure all aspects of the protocol are adhered to in accordance with related Guidelines (such as FDA, GCP, and ICH)
Consults with PI regarding the appropriate administration of investigational product
Under the supervision of the Principal Investigator (PI), prepares and submits regulatory documents in an accurate and timely manner
In collaboration with the PI, incorporates clinical judgment and knowledge of protocol to identify potential study participants according to inclusion and exclusion criteria
Obtains informed consent according to GCP
Schedules subject visits and prepares labs/tests per protocol
Reviews and completes case report forms in timely manner
Conducts the investigational product according to the parameters of the study protocol and under the direction of the Physician
Conducts routine assessments to evaluate the subject’s response to investigational product, and communicates observations to related parties. Also, conducts ongoing assessments of the overall study execution within the facility/practice, communicating concerns to related parties
Educates, informs/updates the subject about the applicable study particulars and details
Documents subject information as it pertains to the clinical study according to the principals of ALCOA (Attributable, Legible, Contemporaneous, Original, and Accurate)
Meets with the study monitor to review, verify and correct all data entered onto the case report form and to ensure appropriate maintenance of study records
Reports consistently on the study, subject’s progress, complaints and issues to PI, study sponsor, or IRB as needed in a timely manner
Notifies PI, study sponsor and IRB of Serious Adverse Events according to protocol
Collects pre-study essential documents according to GCP and files appropriately in the study record
Maintains the study file and subject participant records according to GCP
Ensures appropriate storage, access, and maintenance of records pertaining to investigational product
Assist with various projects as assigned by direct supervisor
Additional responsibilities may include focus on one or more departments or locations. See applicable addendum for department or location specific functions

142

Equity Research Coordinator Resume Examples & Samples

Compile and present necessary industry information from Bloomberg, FactSet, and other industry sources
Create and maintain moderate-to-advanced excel documents, including but not limited to financial models
Assist with database needs, which may involve direct data entry, use of programs for uploading, organizing and manipulating the data in Excel
Assist with various analytical projects; prepare PowerPoint presentations for internal and external audiences and maintain related documents
Maintains calendar appointments, conference schedules and meetings for the research teams. Makes travel and accommodation arrangements, prepares itineraries and coordinates with teams to keep all parties informed of upcoming events, schedule changes, etc
Assists with the planning, coordinating and arrangements for various client and management meetings, luncheons, etc. Anticipates the needs for meeting rooms, menus, travel arrangements, presentation materials, etc

143

Research Coordinator Resume Examples & Samples

Functions as a team player with the department and works effectively with other coordinators in the department to foster an efficient and productive environment for Clinical Research
Implements and conducts multiple research projects in a timely and efficient manner
Prepares/Creates/OA's source documents prior to study start and according to SOP's
Collects data accurately and completes CRF's in a timely manner
Communicates to all appropriate research staff/supervisor/PI, and IRB of any deviations/violations from protocols as necessary
Communicates closely with Regulatory Coordinator to ensure the timely completion of these documents
Prepares on-site monitor visits, including pre-study, initiation and closeout visits
Maintains and updates essential documents as required by the FDA, IRB, Sponsor/CRO or any other regulatory agencies or funding agencies as necessary
Tracks patient visits in the study management software program as necessary
May assist Regulatory Coordinator in the preparation of protocol documents for IRB submission as necessary
Oversees and assists with data clarification forms as necessary and in a timely fashion
Aids in the development of research tools, such as spreadsheets or questionnaires
Develops, implements and continually evaluates patient recruitment strategies for effectiveness
Presents scientific statements or endorsements related to investigational devices/drugs with full disclosure
Provides information to research residents and staff regarding protocol requirements
Submits the IND to the FDA for investigator initiated studies and formulate/track regulatory documents necessary
Assists the staff physician and fellows, or independently writes, abstracts or manuscripts for submission to professional scientific meetings or journals
Performs study-related procedures and visits as required
Conducts follow-up visits of research subjects to evaluate progress and educate them regarding protocol, adverse events and compliance issues as requested
Reviews and documents lab and test results to ensure patient safety

144

Senior Research Coordinator Resume Examples & Samples

Associates Degree in business or related field preferred
5+ years’ experience in related field is preferred
Familiarity with MS Office with a focus on Excel and PowerPoint
Exemplary attendance and job performance

145

Senior Research Coordinator Resume Examples & Samples

Provides technical and functional expertise in the area of Research studies. Recommends appropriate implementation plan. Monitors study routine to ensure progress of studies and reports to PI or Supervisor on progress. Oversees compliance with regulatory and granting agencies
Oversees coordination of a designated study or group of studies. In research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data. Keeps accurate and up-to-date records
May be required to perform phlebotomy, electrocardiograms, or monitor vital signs on study participants. Educates family and contributes to the care and evaluation of subjects, including determining preliminary inclusion/ exclusion criteria. Reports findings to Supervisor or PI
Collaborates with physicians, investigators and other healthcare providers regarding subject care as necessary. Promotes respect for subjects' rights
Administers, scores and evaluates assessments as assigned and as related to study protocol. Collects data, confers with PI and forwards results to sponsor (internal or external)
Collaborates with PI and acts as a liaison between the Food and Drug Administration and drug companies on related issues. Adheres to and trains research staff on Good Clinical Practice, and regulatory and grant agency requirements. Follows protocol as developed. Keeps investigator informed of protocol changes or developments
Oversees availability of drug supplies and/or equipment for studies
Bachelor's Degree, in a field of Science, Behavioral Science or related field, required. Master Degree preferred
Minimum of five (5) years progressively responsible related experience
Demonstrates a high level of scientific knowledge

146

Research Coordinator Resume Examples & Samples

Submission and maintenance of regulatory documents and study records required by the Institutional Board (IRB), the Human Research Protection Office, sponsors and any other regulatory agencies
Participate in screening and recruitment of research study participants
Collect, process and ship specimens according to protocol requirements, in accordance with Haz-mat training and Good Clinical Practice requirements
Become proficient in use of IRB Manager, RedCap and other HIPAA compliant databases for data input and management
You may be required to participate in data collection and analysis
Participate in internal and external regulatory audits
Serve as liaison between PI, research team, study participants and personnel at collaborating institutions
Provide clerical and managerial support for research team as needed
Bachelor of Art or Science or related field
2-3 years experience in human subject research coordination
Strong interpersonal, organizational and communication skills are required
Knowledge of medical and scientific terminology is preferred
Willingness to travel to multiple sites preferred

147

Research Coordinator Resume Examples & Samples

Bachelor’s degree or significant experience in research coordination
Minimum 3 years’ experience in a related area
Washington State Medical Assistant-Registered will be required with Swedish Medical Center facility application completed within 7 days of hire. Must obtain active license within 60 days of hire
Advanced knowledge of FDA research policies, other applicable federal regulations and/or GCP guidelines
Expertise in standard office software packages (Word, Excel, PowerPoint, etc.)
Familiar with and comfortable with research methodology and the “scientific method”: for conducting research projects
MA-R not required prior to hire
Certified Clinical Research Coordinator (CCRC) or similar professional research certification

148

Research Coordinator Resume Examples & Samples

Bachelor's Degree in Science, Healthcare, or related field. Significant experience in research coordination can be substituted for education
Minimum one year of experience in related field
Basic knowledge of FDA research policies
Must be well versed in scientific terminology
Familiar with research protocols and standard study requirements
Washington State Medical Assistant-Registered will be required with Swedish Medical Center facility application completed within 7 days of hire. Must obtain license within 60 days of hire

149

Research Coordinator Resume Examples & Samples

Primary anticipated responsibilities include: Data collection and management; Statistical analyses; Literature review; Contributing to computer simulation modeling efforts (developing and running computer models) The opportunity exists to participate in scientific manuscript preparation and writing. Support of manuscript preparation (e.g. communications with co-authors, Table/Figure development) is expected
A strong interest in medicine or medical research as a career
A strong interest in participating in clinical medical research
Proficiency with Microsoft Word and Excel, some familiarity with statistical and or database management software
Willingness to learn and work with computer-based simulation models
An ability to perform medical literature searches
Strong database management skills, for data extraction from national or local patient databases
Excellent communication skills, including ability to interact with physicians, patients and researchers
Strong work ethic, excellent organization skills, and meticulous attention to detail

150

Bft Research Coordinator Needed for Mgh Surgery Resume Examples & Samples

Serves as office liaison between Institutional Review Board (IRB) and Lab safety, processing requests for new research protocols, completing continuing reviews for ongoing studies and submitting amendments for any changes to a study
Prepares service contracts and standing purchase orders as well as material transfer requests
Prepares and organizes materials for internal and external dissemination
Schedules meetings, updates calendars and makes travel arrangements
Answers telephones; places/returns telephone calls as requested
Retrieves, screens and triages office mail
Performs photocopying, faxing, filing as requested
Orders office supplies, forms, stamps, etc. as needed and maintains spreadsheet of all orders
Performs check requests, coordinates travel arrangements and prepares reimbursement materials
Arranges for outside visitors, medical students, etc. as requested
Participates in weekly CORE staff meetings by preparing agenda and facilitating meeting
Performs/participates in special projects as may arise from time-to-time
Ordering and picking up food supplies for laboratory
Completing onboarding and HR paperwork for incoming interns and trainees
Maintenance of lab website
Associates degree required with Bachelor’s degree helpful. Microbiology and/or Molecular Biology skills a plus
Ability to multitask and work accurately
Neat and orderly work habits
Management of IRB documentation
Coordinating events/meetings
Exceptional computer skills (including MS Word, Outlook, Internet, and Spreadsheets)
Is knowledgeable and compliant in all hospital, State and Federal regulatory requirements including HIPAA, Joint Commission

151

Melanoma Translational Research Coordinator Resume Examples & Samples

Incumbent will supervise post-doctoral fellows and research technicians in the Flaherty lab
B.A/B.S. required
Minimum of 3-4 years related experience required
Proven success and experience facilitating multi-disciplinary interaction
Ability to work independently with general direction, moderate oversight and day-to-day instruction
Ability to handle multiple complex projects simultaneously
Commitment to excellence
Demonstrated ability to take initiative based on sound judgment
Knowledge of MGH/Partners/HMS conflict of interest rules
Flexibility and willingness to take on broad range of tasks
Demonstrated ability to work effectively with colleagues at all levels, from administrative assistants to academic, hospital, and corporate collaborators

152

Research Coordinator Resume Examples & Samples

Assist in data collection, quality review of data, data analysis and data presentation and publication
Coordinate and administer questionnaires, and assist with procedures for obtaining patient screening and recruitment as needed
Coordinate and perform duties for approved research projects according to defined protocols and procedures
Coordinate recruitment efforts, training, and supervise research staff as needed
Follow appropriate research policies and procedures including all applicable laws and regulations and maintains scientific integrity including accurate data storage
Follow the mandatory reporting procedures for any incident or serious event that did affect or potentially could have affected the clinical care of any patient/participant
Revise, renew and maintain IRB approval, protocols and consent forms for studies
Masters degree in psychology, health administration, or other related field is required
Five years of relevant research and/or administrative experience in a clinical or academic setting is required
Prior supervisory experience strongly preferred
Computer Skills (Microsoft Office Products)
Excellent communication skills both verbal and written

153

Research Coordinator Resume Examples & Samples

Provide administrative assistance and support to TM Labs Leadership as needed
Draft, prepare, and send meeting invitations on behalf of TM Labs Leadership
Assist in the editing of presentations and reports to ensure high-quality deliverables
Maintain/Update the TM Labs Portal (SharePoint)
Assist with internal and external outreach as needed to support TM Labs projects
Work with the Chief of Staff to ensure TM Labs deadlines and commitments are met
Compile monthly progress reports on TM Labs projects
Support Research Scientists and Consultants on various project needs
Organize materials into online repositories
Create supporting documents for research processes and activities
Develop data dictionaries and keeping records for key data sets
Coordinate interactions between TM Labs staff and internal stakeholders
Effective time management skills and ability to work well under pressure
Excellent organization, multitasking, and prioritization skills
Excellent written and oral communication skills; equally comfortable working via email and phone
Ability to work across teams and build relationships with staff at all levels
Demonstrated experience using Microsoft Office, specifically Outlook, Excel, and PowerPoint
Superior problem solving ability; ability to learn substance of research quickly
Demonstrated initiative, persistence, and resourcefulness

154

Research Coordinator Resume Examples & Samples

Bachelor's degree (preferably in science, healthcare, or other related field). Significant experience in research coordination may be substituted for educational requirements
Minimum of three years experience in related area
Expertise in standard office software packages (Word, Excel, PowerPoint, etc.), standard office equipment (photocopiers, facsimiles, telephones, pagers, etc.)

155

Research Coordinator Resume Examples & Samples

1) BA/BS in psychology, biology, engineering, or related field
2) two years of research experience
3) demonstrated organizational skills or experience with data management
4) desire to succeed in a fast-paced research environment with multiple duties
5) Demonstrated attention to detail, organizational skills, and excellent written and oral communication skills
6) Proficiency with Word, Excel, and PowerPoint or equivalent
1) Proficiency with MATLAB, statistical analysis, and/or experience with web development
2) Experience with writing and following IRB protocols

156

Research Coordinator Resume Examples & Samples

Organizes study related activities to ensure compliance with FDA, GCP, IRB, HIPAA, SOPs, sponsor and institutional regulations and requirements.Serves as contact for subjects, study personnel, the department, the school, pharmacy and other ancillary service departments, Institutional Review Board (IRB) and study sponsor
Pre-screens patient records and assesses patient eligibility. Coordinates study participant activities including screening, recruitment, orientation, correspondence, and ongoing patient education about clinical trials. Schedules and confirms subject appointments, tests and procedures with internal and external providers as needed. Coordinates with labs, pharmacies, hospitals and other ancillary units for protocol required tests/procedures/drug administration/reimbursements for upcoming patient visits
Collects patient data, inputs and analyzes for research studies. Maintains accurate, complete and timely records, including source documents, consent forms, case report forms, protocol documents, and regulatory documents, as required by sponsor and institutional guidelines
Coordinates with labs for sample and data collection, sample processing and shipment for each study. Orders supplies and equipment. Researches and develops recommendations for new supplies/equipment purchases
Tracks, reports, documents and enters data internally and in sponsor’s system for patient visits and study status.Provides updates to and resolves queries with ancillary departments including the accounting department
Submits protocols to IRB, completes study continuing review, amendments, and reportable events to IRB in a timely and accurate manner, and closeout the study with IRB
Schedules, prepares and participates in initiation and closeout visits, monitoring visit and external/internal audits. Provides timely response to queries from sponsor and/or auditors, and close the study with sponsor
Participates in research meetings with PIs to present research updates and gather future research plans. Regularly meets with the department to provide research/workload updates and discuss potential issues and plans
Documents and improves standard operating procedures, researches and prepares guideline documents and reports as assigned
Assists in organization and preparation of grant proposals. Gathers documentation such as annual reports and detailed budgets for inclusion in proposal. Assists investigators in developing research proposals and budgets. Interfaces with funding and regulatory agencies to exchange information

157

UX Research Coordinator Resume Examples & Samples

1-2 years experience in coordinating tasks that support research activities, including: participant recruitment, scheduling, and communication
Detail-oriented, organized, resourceful, and able to work independently
Strong interpersonal, communication, and collaboration skills
Proficiency with Google office productivity tools, including email, calendar, spreadsheets, word documents, and presentations
Interest in user experience research and design

158

Research Coordinator Resume Examples & Samples

Master's level or higher degree, or equivalent combination of experience and education in public health, gerontology, or related field
Demonstrated experience in writing/editing and submitting manuscripts for publications and scientific journals
Demonstrated ability in writing grants and research proposals
Knowledge of the contract and grant proposal submission process to federal, state or private funding organizations, including the online submission process
Demonstrated experience in coordinating a research project
Knowledge of human subjects and Institutional Review Board and other federal research policies and procedures
Attention to details and ability to analytically assess and compile written responses
Experience in multi-tasking and ability to perform under stress and deadlines
Knowledge of UCSD policies and procedures

159

Technical Research Coordinator Resume Examples & Samples

Limited position, may become career**
Demonstrated knowledge and skill in current and emerging Internet and social media platforms
Some expertise in computer science and engineering
Social and team-oriented
Extremely organized and detail-oriented
Online/social media marketing and Technology knowledge
Experience either as a journalist or as an author/co-author on previously submitted/published research-related manuscripts
Master's Degree and at least 2 years of project management experience

160

Research Coordinator Resume Examples & Samples

Ability to confidently and independently write research manuscripts and briefs that will convey our research to local clinics and organizations
At least 2 years of research experience carrying out behavioral interventions
Demonstrated knowledge and skill in the use of social media platforms
Demonstrated statistical analysis skills in order to analyze research results to determine study outcomes
Ability to establish and maintain cooperative working relationships
Willingness to work occasional evenings and weekends
Organizational skills to maintain records and coordinate other tasks as required
Ability to communicate with others about sensitive behavioral issues, including drug use and criminal behavior, and frequency of high-risk behaviors
Skill in speaking and writing to persons of various social, cultural, economic, and educational backgrounds
Demonstrated knowledge of personal computers and relevant software programs (e.g., data entry, word processing, spreadsheets)
Willingness and ability to maintain confidentiality of subjects
Ability to communicate clearly and effectively, verbally, and in writing, with subjects, staff, and supervisors
Skilled in keeping accurate and timely records
Ability to work independently and report to Principal Investigator on a regular basis and in a timely manner
Ability to manage competing demands/assignments/deadlines
Ability to be punctual and maintain a satisfactory attendance record
College or graduate degree strongly preferred
Bilingual English/Spanish
Experience in data entry and cleaning
Experience working with substance abusers and/or with HIV-positive populations

161

Background Check Research Coordinator Resume Examples & Samples

Make sound employment adjudication decisions to mitigate legal risk
Adhere to all department guidelines and procedures
Regular, dependable attendance & punctuality
High school diploma or general education degree (GED) required
Prior experience in conducting applicant interviews and/or pre-employment screening preferred, but not required
Ability to collaborate with outside vendors and internal clients at all levels
Basic math functions such as addition, subtraction, multiplication and division
Must be able to work independently with minimal supervision
Retail business acumen; understanding how retail organizations operate and how roles work together
Must possess the ability to prioritize a changing workload, with a high sense of urgency

162

Assistant Clinical Research Coordinator Resume Examples & Samples

BA/BS in Psychology, or related field of study
Research experience, preferably with eating disorders
Good understanding of psychopathology and DSM V diagnoses
Comfort with working with children and their families

163

Research Coordinator Resume Examples & Samples

Administer questionnaires, and assist with procedures for obtaining patient screening and recruitment as well as obtaining research specimens
Assist in data collection and data entry and quality control of data
Assist in hypothesis generation, data collection, data analysis and data presentation and publication
Complete online IRB certification modules 1 and 2 (Research Practice Fundamentals) in accordance with Health Sciences at the University of Pittsburgh
Follow the mandatory reporting procedures for any incident or serious event that did affect or potentially could have affected the clinical care of any patient
Perform duties for approved research projects according to defined protocols and procedures including appropriate collection, recording, and storage of data
Process, label, store and ship blood specimens obtained from research subjects
B.A. degree, or equivalent combination of experience and training - including 3-5 years of experience in coordinating multiple aspects of research projects (patient recruitment, assessment, treatment planning, and data collection,) required
Previous multi-center Clinical Trial experience is strongly preferred
Working knowledge of Research regulations and IRB protocols is strongly preferred
Ability to accurately collect, and store research data
Demonstrated ability to effectively communicate with patients, staff and investigators as well as maintain patient confidentiality
Ability to work independently, must be able to work a flexible schedule based on study needs
Ability to interact with patients/study participants and research and medical staff
Knowledge and skills necessary to provide care and/or interact appropriately to the ages of the patients served by his/her assigned unit as specified below
Knowledge of the principles of growth and cognition over the life span and possess the ability to assess data reflective of the patients status and interpret the appropriate information needed to identify each patients requirements relative to his/her age-specific needs and to provide the care needs as described in the departments policy and procedures

164

Research Coordinator Resume Examples & Samples

Should have prior experience with coding behavior observation using a qualitative analysis software
Interest and enthusiasm for topics related to child development and health
Ability to work several hours coding observation data

165

Research Coordinator Resume Examples & Samples

Ability to work both independently and collaboratively
Knowledge and application of scientific procedures and research techniques
Ability to mentor others

166

Research Coordinator Resume Examples & Samples

Schedules subjects for protocol-related evaluations. Collaborates with physicians, investigators and other healthcare providers. Promotes respect for subjects’ rights
Bachelor’s Degree, required
Redcap preferred
Prior Clinical Trial or Sponsor Trial experience, preferred
Ability to take initiative and work interdependently, meet deadlines with a sense of urgency, multitask, adjust to shifting priorities and work under defined rules and regulations

167

Research Coordinator Lead-swedish Cancer Institute Resume Examples & Samples

Bachelor's degree required, preferably in science, healthcare, or other related field. Significant experience in a supervisory capacity may be substituted for educational requirements
Washington State Medical Assistant-Registered will be required with Swedish Medical Center facility application completed within 7 days of hire. Must obtain active license within 60 days of hire. Employee will not be authorized to practice independently until registration is obtained
Minimum of seven years experience in related area
Certified Clinical Research Coordinators (CCRC) or similar professional research certification preferred

168

Lead Clinical Research Coordinator Resume Examples & Samples

Serves as liaison between clinical research team and hospital/research institute senior leaders. Provides strategic direction on clinical research portfolio and clinical research pipeline, issue resolution and quality improvement initiatives
Interfaces between clinical staff, the Office of Sponsored Research, Research Administration, PIs, clinical research staff, and external entities to create and adhere to programmatic budgets and strategic plans
Interfaces with clinical staff to identify patients eligible for clinical trials across one or multiple sites of service
Interfaces with patients and their families to provide education regarding investigational studies, and requirements of participation to assure they are informed prior to obtaining written consent. Completes required follow-up and active patient monitoring per study protocol at one or multiple sites of service
Plans, coordinates, and manages all activities pertinent to the specific clinical trials, ensuring patient safety, good clinical practices, and compliance with the protocol and regulatory agencies
Bachelor's degree or RN/BSN; Master's degree preferred in related field
Generally has at least 6 years of related experience
Current research-related certification from accredited program (e.g. CIRA, CCRP) required or ability to obtain within 6 months of hire
Role models clinical research operations and interfacing with PI/clinical research team; has proven track record of fostering relationships with external constituents; demonstrates in- and out-patient clinical issue resolution; has worked to develop a research presence nationally (e.g. publications and presentations)
Follows standard and/or other appropriate precautions using personal protective equipment as required

169

Senior Clinical Research Coordinator Resume Examples & Samples

Interfaces between clinical staff, the Office of Sponsored Research, Research Administration, PIs, clinical research staff, and external entities to identify clinical research pipeline and completes protocol budgeting, feasibility, and initiation
Provides in-service education to the appropriate hospital personnel in the departments involved with the investigational study
Interfaces with patients and their families to provide education regarding investigational studies, and requirements of participation to assure they are informed prior to obtaining written consent
Completes required follow-up and active patient monitoring per study protocol at one or multiple sites of service
Bachelor's degree or RN/BSN
Generally has at least 4 years of related experience
Current research-related certification from accredited program (e.g. CIRA, CCRP) required or ability to obtain within six months of hire
Driver's license may be required depending on facility requirements
Has mastered the components of clinical research operations, works with PIs/clinical research team and clinical teams to resolve issues, initiates new clinical research trials, sets study budgets, and serves as a point person for external constituents

170

Market Research Coordinator Resume Examples & Samples

Maintain the Group Rooms Control Log (GRC) and FDC database
Daily logging and distribution of all incoming leads, Generate the Weekly and End of Month Sales Reports
Prepare and distribute monthly production forecast, Enter pick-up on a daily or weekly basis
Must have full knowledge of the Sales Administration Manual and ensure that procedures are being followed
Responsible to maintain monthly recap with reservations to insure GRC blocks are the same as Reservation blocks
Assist in 90 day forecasting process, Attend Weekly Support Staff Meetings
Types and distributes all correspondence, including letters, emails, proposals, contracts, etc. for assigned managers
Ensures that all correspondence is 100% accurate
Maintains account files and ensures that all information is included in file, i.e. post-convention reports, letters, fax information
Professionally answers calls to the sales office and accurately takes messages, as applicable
Enters group information (sites, resumes) in computer database
Assists in generating proposals with information accurate and specific to each client
Creates and updates documents and spreadsheets for DOSM, as needed
Takes detailed inquiry leads and submits to appropriate manager
Inputs amenities into compute for VIP clients and processes paperwork (amenity card, receipt signature from Room Service.)
Orders office supplies and maintains function of office equipment
Good verbal/written communication skills
Maintain a professional business appearance, attitude, and performance
Ability to effectively use Microsoft Word, Publisher, Outlook, and Excel is required
Must have good organizational skills, attention to detail and be able to multitask
Previous hospitality or administrative experience is required
Experience in a sales environment is strongly preferred

171

Research Coordinator Resume Examples & Samples

Experience as a research professional for investigator-initiated research projects, with expertise in grant and protocol management including oversight of daily research operations
Excellent written and verbal communication, including patient interactions, consulting, and customer service skills
Proficiency with standard MS Office software, including Word, Excel, Access, and Power Point
Strong internal and external customer service skills
Ability to adapt and respond appropriately to competing priorities in a fast-paced environment
Self-motivated, self-starter who takes initiative to improve existing processes

172

Senior Clinical Research Coordinator Resume Examples & Samples

With direction from the PI, oversees study operations for all NeuroNEXT studies
Establishes and monitors timelines and benchmarks for study implementation, recruitment, and completion
Coordinates and supervises efforts for all NeuroNEXT studies and provides guidance to the study specific staff on required network training, protocol compliance, meeting recruitment goals, performing study procedures and managing data collection
Monitors study performance for subject enrollment goals and data acquisition in accordance with the protocols and conveys information to NeuroNEXT PI
Serves as primary resource for all regulatory and operational aspects of the NeuroNEXT site, overseeing submission and maintenance of documentation to the CIRB
Interacts directly with involved staff at the UM sub-sites (MCH and JHS), study sponsors and monitors, the NINDS, other network sites, the Clinical Coordination Center, and the Data Coordination Center
Designs and implements quality assurance systems to assure protocol compliance
Ensures compliance with applicable NeuroNEXT, FDA, NIH and other regulatory agencies' requirements
Develops and maintains Standard Operating Procedures for the UM site
Oversees collection and integrity of trial data at the site
Serves as the primary site liaison and appropriately triages correspondence to relevant parties
Meets regularly with investigators and coordinators involved with NeuroNEXT trials
Supports local research infrastructure by organizing monthly Neurology Clinical Research Roundtable sessions, raising awareness about the network, and engaging faculty in network initiatives
Assists with budget monitoring of NeuroNEXT study funds

173

Market Research Coordinator Resume Examples & Samples

Assist with the development of sales presentations and marketing strategies
Administrative support including phone coverage, internal brand/hotel and client communication, travel coordination, expense reports and tracking, marketing calls and meeting preparation (prepare weekly minutes from internal meetings) and follow-up as well as other administrative tasks
Maintain and update revenue production from marketing campaigns
Assist with the development of internal and external presentation materials including PowerPoint presentations, webinar content, advertisements, marketing and collateral
Maintain balance sheets, expense checkbooks and invoices
Assist with other projects as needed
Strong attention to detail, well-organized and ability to deal efficiently under pressure and multi-task while being personable
Highly skilled with Microsoft Excel, including the ability to use filters and pivot tables
Proficient with MS Word, MS PowerPoint and MS Outlook
2-4 years of administration experience preferred but not required
College degree or equivalent required

174

Research Coordinator Resume Examples & Samples

Preparation and design of research and study projects
Capacity building for research and study team
Research and Study implementation
Data Management and analysis of study and research results
Experience in design and implementation training/Capacity-building strategies on nutrition interventions, especially maternal and child nutrition
Effective in written and oral communication; be able to speak and write with a standard of English
Computer literate in MS Word, MS Excel, MS PowerPoint, e-mail and internet
Familiarity with the Ministry of Health policies and programs aimed at improving nutritional status of women and children
If you cannot see the job announcement on World Vision website through the link above(1): Please copy job ID: NO-FY17-F017 to be your email subject ONLY and attach your completed Application Form, CV and Cover Letter to Email: cam_recruitment@wvi.org or contact us at Tel: 023 216 052 Ext: 121

175

Research Coordinator Resume Examples & Samples

Conceive, author and edit grant proposals, exhibiting strong expository as well as persuasive prose. Possess a high-level command of grammar and spelling
Conceive, plan and conduct research for trauma grant opportunities and funding using advanced search techniques. Possess proficiency in searching funding sources through on-line databases and printed resource material. Filter grant-making prospects and project feasibility of funding
Assist the members of the Division of Trauma Surgery and Surgical Critical Care in the development of documents and proposals in response to Requests for Proposals from private foundations and governmental funding sources. Includes preparation of the RFP
Customize grant proposals in accordance with each grant-making organization’s preferences and follow exactly each grant-making organization’s guidelines
Prepare project reports, financial and statistical reports, surveys, documentation and analyses as required by grant-making organizations to ensure compliance with all requirements
Communicate and report regularly with the Chief, Division of Trauma Surgery & Surgical Critical Care, Director of Trauma Center & Trauma Program, on the status of these activities
Facilitate and enforce adherence to research deadlines
Exhibit superior communication and information gathering skills to work as a team playerin the smooth operation of an active and highly visible academic program
Develop and compose various non-routine communication pieces to include: solicitation letters, case statements and funding proposals
Acquire and maintain sound knowledge and understanding of the CHI Health Creighton University Medical Center and the projects, programs, services, equipment, technology and/or capital needs for which funding is sought
Manage information ethically, accurately and confidentially
Maintain a professional attitude with patients, visitors and other hospital personnel while assuring confidentiality of patient information and other hospital information
Complete grant, journal, and publication writing duties and responsibilities as assigned. Maintain standards of publication and authorship
Work effectively and collaboratively in a diverse and multi-cultural environment
Maintain academic and clinical professionalism, including interactions with collaborating academic centers and departments and with patients/families
Build and maintain databases as required by grantees and work product
Reports regularly to the Chief, Division of Trauma Surgery & Surgical Critical Care, Director of Trauma Center & Trauma Program
Two - five years’ experience in clinical research
Two – five years’ experience in administering grant projects
Ability to work independently without supervision
Demonstrated advanced computer skills/expertise using Microsoft Word, - Excel, PowerPoint, Access and grant management software
Strong knowledge of clinical grant management
Excellent oral and written communication skills, excellent knowledge of grammar and sentence structure
Excellent listening, problem solving and planning skills
Enthusiasm for, and understanding of, building external relations
Strong leadership and motivational skills
Strong skills in human relations and diplomacy
Ability to work efficiently and independently on multiple simultaneous projects
Ability to think critically and creatively
Bilingual or multilingual skills preferable (not required)

176

Research Coordinator Resume Examples & Samples

The first is ensuring placement of clinical trials within targeted and appropriate dialysis units or CKD practices
The second is organizing resources including PIs
The third is overseeing the execution of the studies, ensuring successful completion within GCP, with minimal participant attrition
The fourth is mentoring and involving the right TMs in the village to assist in study execution
The fifth is participating in the cultivation and nurturing of physician relationships
Individuals who take on the role of Regional Study Coordinator generally have some defining qualities. These qualities include the ability to manage complex and strategic projects with a focus on core task accomplishments. This individual will have a drive to continuously educate themselves and understand both clinical and regulatory components of clinical trial execution. They will also possess the ability to communicate well, be tenacious, flexible, and versatile
Provides overall management and execution of studies as assigned
Ensures DVA sites are committed to the project
Leads study team
Acts as a liaison between the physicians, sponsors and TMs
A deliverable revenue/ebitda goal for each budget year
Mentor and build the capacity of village TMs to assist in the conduct of clinical trials
Performance-based rewards based on stellar individual and team contributions

177

Research Coordinator Resume Examples & Samples

Must have excellent organizational and interpersonal skills
Must possess excellent written and verbal communication skills
Must have ability to multi-task and work independently
Proficiency using software programs such as Microsoft Office (i.e. Word, Excel, PowerPoint, and Outlook)

178

Research Coordinator Resume Examples & Samples

Oversee the work of healthcare analysts, biostatisticians, and Medicaid policy experts in synthesizing results from qualitative and quantitative data
Lead deliverable production to ensure that internal and external reports and/or deliverables adhere to project specifications, are submitted on time, and meet or exceed quality standards. Develop quarterly progress reports for the sponsor
Write reports and develop complex charts, tables, and presentations from synthesized information that is provided by bio-statisticians and senior faculty in the team. Assist with interpretation of results and development of program/policy recommendations
Oversee data requests and data collection from partner state agencies and supervise administrative staff assisting with project coordination
Develop and maintain a comprehensive project plan to guide the day-to-day tasks, operations, and communications. Build and manage relationships with vendors for qualitative data collection
Master's Degree in social/behavioral sciences, public health, or related field and five or more years of professional experience
Previous experience in health policy research and/or evaluation of healthcare programs is strongly preferred
Experience with research project management is a plus
Demonstrated experience with writing of complex reports
Ability to work independently and ability to collaborate with external constituencies
All applicants should have clear ability to take initiative and manage time

179

Research Coordinator Resume Examples & Samples

Theoretical knowledge of biomedical informatics, computer science or related field as typically acquired by a Bachelor's degree, or an equivalent combination of education and experience
Demonstrated experience organizing large volumes of data using creative tools, logs and databases created to use with multiple research projects
Demonstrated experience interpreting/coordinating research protocols and the corresponding data requirements. Demonstrated experience with human subjects research and processes
Demonstrated knowledge of library referencing procedures, knowledge of PubMed searches and Reference Manager. Demonstrated experience conducting literature reviews and internet searches for project-related clinical studies
Demonstrated experience with grant proposal preparation, agency rules and regulations, particularly NIH
Experience with website content management
Demonstrated experience with multiple computer programs such as Microsoft Office (Excel, Word, Outlook, Power Point, and Project), Adobe (Photoshop, Acrobat, and Illustrator), EndNote or equivalent, SharePoint, Joomla or equivalent, and Camtasia or equivalent
Strong decision making skills and ability to use independent judgment and discretion to quickly set priorities and establish new procedures when needed. Demonstrated ability to research, analyze, recommend, communicate, and implement solutions. Must function independently with minimal direction
Experience with event planning, outreach, and social media marketing

180

Research Coordinator Resume Examples & Samples

Creation of site-specific SOPs
Monitor on-line recruitment
Manage and schedule follow-up as specified per protocol
Complete, organize and maintain all study documentation as directed by the supervisor

181

Donor Database & Research Coordinator Resume Examples & Samples

Ensure prompt and accurate processing and documentation of donor gifts, integrating with Financial Edge software, complying with IRS regulations and department procedures
Develop and produce queries, donor profiles, dashboards, custom reports, and mailing lists to support department goals. Manage any data mergers
Make recommendations on data organization and integrity; develop best practices; train staff in best practices and enforce procedures
Create and process prompt donor acknowledgement letters to include: thank-you’s, honor/memorial gifts, new and lapsed donor reports, pledge and past-due reminders
Use Kintera Sphere software to create and update online donation portals and registration webpages
Work closely with finance department to reconcile all gifts and records
Conduct prospect research in coordination with development team. Research and master tools to facilitate this process. Manage research and prospect modules in Raiser's Edge
Assist in event planning using data management skills, which may include: invitation and mailing lists, registration and financial tracking, and specific guest correspondence
Coordinate all software upgrades with HCMC IT department
Serve as the key contact and administrator to Blackbaud to maintain Raiser's Edge and all relevant modules. This includes maintenance, upgrades and system changes
May provide work direction for future data entry staff
Bachelor degree in a related field or an approved equivalent of education and experience
Experience with prospect research tools, mailing list acquisition and management, fundraising analysis and reports
Systems expert and ensures accountability to structured processes
Ability to manage workload independently and build a network of resources
Knowledgeable of best practices within donor relations
Strong communication and diplomacy skills
Assertive and able to push back when appropriate
Collaborative and effective team player across diverse groups
2 years experience in donor database management and Raiser's Edge highly preferred
Experience with safety net hospitals preferred

182

Practice Research Coordinator Resume Examples & Samples

Ensures availability of drug supplies and/or equipment for studies. Maintains drug accountability logs
Bachelor’s Degree, in a field of Science, Behavioral Science or related field, required
Certified in Haz-Mat Training for packing and shipping, as needed per study protocols, required
Certification required for performance of venipuncture, electrocardiogram and vital signs, as needed per study protocols

183

Research Coordinator Resume Examples & Samples

Knowledge of Microsoft Office (i.e. Word, Excel, Outlook, PowerPoint) and Atlas.ti
Skill in completing assignments accurately and with attention to detail
Strong interpersonal skills needed to interact with potential research subjects
Ability to troubleshoot and problem solve

184

Research Coordinator Resume Examples & Samples

Monitors research processes to ensure data quality is in accordance with corporate standards
Verifies market analytical reports related to transactions, vacancy, development, absorption, rents, tenants, and leasing activity
Delivers statistical and analytical reports as required by leadership and sales professionals
Assists in training staff, management, and sales professionals in the use of research tools and resources

185

Research Coordinator Resume Examples & Samples

Responsible for coordination of a designated study or group of studies in a clinical or laboratory based research project. In clinical research projects, oversees recruitment of subjects, implementation of study procedures, and the collection, processing and analysis of data. In laboratory research, oversees and/or performs the scheduling of experiments, and the collection, processing and analysis of data and blood specimens. May be required to perform venipuncture on study participants
In clinical research, may ensure the safety and comfort of patients being evaluated; supervises the scheduling of patients for clinical and biological evaluations; sets up educational workshops for patients and families. In laboratory research, orders reagents and supplies as needed for experiments, schedules personnel, ensures access to research equipment
Administers and scores assessments such as functional disability ratings, side effects evaluations, neurocognitive measuring and/or other clinical ratings
Interfaces with the Research Grants Office; in clinical research with the Human Subjects Review Committee; and, as necessary in laboratory research, the Animal Care and Use Committee. In both clinical and laboratory research, organizes all phases of grant process for submission to funding agencies. Related responsibilities include the editing of manuscripts, grants and scientific articles and presentation
In clinical studies acts as liaison between the Federal Drug Administration and drug companies on related issues. Oversees availability of drug supplies and equipment for studies
Knowledge of Psychology, Basic Statistics and Research methods as normally acquired through completion of a Bachelor’s Degree in Psychology or related clinical field, required
Minimum of two (2) years progressively responsible related work experience to ensure working knowledge of research methods and analysis
Certified in Phlebotomy, required for venipuncture preferred

186

Research Coordinator Resume Examples & Samples

Demonstrated research administration experience and understanding of applicable principles
Working knowledge and understanding of programs and processes of primary granting agencies, to include, but not limited to, NIH and other federal, state and private foundation regulations and requirements, as well as corporate and private sponsors
Significant experience in office workflow management at the senior level with excellent organizational skills and the ability to change priorities quickly and often with little or no disruption to operations
Ability to work in a self-directed manner, demonstrate initiative and maintain a high degree of accuracy and attention to the smallest detail, with exceptional analytical and organizational skills
Working knowledge and understanding of an academic medical healthcare environment
Skill in program development and implementation; including and providing guidance in project management
Experience with planning, executing and evaluating programs, meetings and conferences successfully, including project management to include: developing project budgets; vendor selection; site selection; and, contracting
Ability to effectively communicate, with excellent oral and written communication skills
Experience with database systems. Demonstrated superior skills using Excel, Word and other Microsoft Office software applications
Experience developing and maintaining presentations and executive correspondences. Database management skills including the ability to create and query reports
Ability to gather, organize and maintain data and a proficiency in graphing, data-entry, spreadsheet, presentation software and other technical applications
Ability to work in a team environment, with demonstrated ability to work independently with limited supervision and ability to work toward common goals as part of a lager administrative team
Experience working within the University of Florida academic system is a plus, but not required
UF financial security clearance and ability to obtain VCU purchase card required
Must be able to interact with faculty, laboratory staff, students and visitors in a highly diverse environment – in person, via written communications, and on the telephone – with a high degree of professionalism

187

Research Coordinator Resume Examples & Samples

Manage and monitor all aspects of assigned projects. Including supervision of other research personnel supporting the project as needed
Coordinate and/or perform literature reviews and other information queries to assist faculty as needed to enhance their scholarly activity
Establish and maintain an understanding of and relationships of potential funding sources for specific projects and/or programs associated with the scholarly activities of the faculty
Other contract and grant duties as assigned by Director and/or PIs

188

Undergraduate Research Coordinator Resume Examples & Samples

15% Enhance awareness about undergraduate research opportunities through courses, off and on campus events, workshops, etc
10% Update undergraduate research program website and undergraduate research list serv on a regular basis
10% Design and implement student outreach for undergraduate research opportunities and recruitment of students from groups traditionally under-represented in research. Serve as liaison to OSU academic advisors and faculty regarding promotion of undergraduate research
10% Develop vision and strategy, in conjunction with academic units, committees and OSU leadership, for the promotion and expansion of undergraduate participation in research, scholarship and the arts as an integral component of OSU’s educational programs
10% Pursue grant and other funding sources to support undergraduate participation in research
10% Research and report on program activities as well as national trends and best practices in undergraduate research and experiential learning

189

Research Coordinator Resume Examples & Samples

May develop market research graphics for assigned specialty groups and gathers statistics and data from outside sources
If necessary, coordinates requests and responses between the local office and Company resources
Bachelor’s degree preferably in geography, urban planning, marketing, or business administration
Minimum of 1-2 year’s experience working in an office environment preferred
Familiarity with basic concepts of demographics and cartography
Strong organizational and multi-tasking skills
Strong PC skills in working with spreadsheets, database management and/or graphics packages
Strong initiative and self-reliance, ability to work independently
Ability to work various individuals at various levels of management

190

Senior Clinical Research Coordinator Resume Examples & Samples

Feasibility Assessment and Site Selection Process: Coordinate tour of facilities for sponsors
Site Initiation Process: Participate in sponsor-related site initiation visit. For PI initiated studies, assist PI in developing Site Initiation process
Enrollment of Patients: Identify patients for that meet criteria for protocol. Screen and consent patients for study
Treatment Phase: Provide clinical services as required including patient assessments, distribution of medications, collection of specimens, and timed blood collections (PKs). Appropriately document these encounters. Ensure that protocol-specific tests, scans, etc are scheduled and promote patient compliance to protocol regimen
Education of Patients: Educate patients about the study. Be available to answer patient’s questions and assist them when necessary
Adverse Events: Identify and access clinical adverse reactions and events. Notify appropriate parties of adverse events
Advocate for Patient: Advocate for patient’s well being

191

Senior Clinical Research Coordinator Resume Examples & Samples

Conducts clinical testing, develops protocols and assures all protocol procedures are approved
Bachelor's degree in sciences or related field. Master's degree preferred
5 years of clinical research Excellent written and oral communication skills
Demonstrated leadership potential

192

OB / GYN Research Coordinator Resume Examples & Samples

Manages all aspects of conducting clinical trials
Act as liaison between the investigators, primary care providers, the Institutional Review Board (IRB), the Office of Clinical Research (OCR), and the sponsor
Along with the investigator, will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study
Responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files

193

Research Coordinator Resume Examples & Samples

This position will serve as administrative and data support to the primary investigator, state project director, data and advisory groups
Excel knowledge and analysis is essential, the Coordinator will be responsible for analyzing data and developing charts/graphs for presentations
Manage communications for all stakeholders including meeting and communication updates, Website maintenance, branding and event planning
Assist in background research for the proposed quality improvement projects and support toolkit development for hospitals across IL
Be accountable for monitoring the safety and well being of all study participants

194

Research Coordinator Resume Examples & Samples

Bachelor’s degree in sustainability, environmental science, business or related field
Experience working with and reviewing technical materials
Experience interacting with technical staff
Experience driving projects to completion on time
Master’s degree in business administration, sustainability, environmental science, engineering, or related field
Experience leading meetings with technical staff both in person and via webinar
Experience managing projects with Microsoft SharePoint
Experience/knowledge regarding sustainability for consumer goods and supply chains
Experience coordinating technical projects between multiple locations, time zones and work schedules
Excellent communication skills both in person and via email
Ability to work with colleagues located in multiple offices
Ability to present processes and procedures to technical staff in Microsoft Powerpoint
Ability to understand and create technical content
Ability to communicate in an open and understanding manner
Ability to drive projects to completion on time
Ability to organize and analyze large amounts of information using Excel

195

Research Coordinator Resume Examples & Samples

Experience in research with knowledge about the conduct of clinical trials, research principles, and methodologies/study design
Bachelor’s degree in Health or Biological Sciences
Working knowledge of state and federal regulatory guidelines related to research
Good computer skills including working knowledge of a PC and Microsoft Office (Word, Access, and Excel)
Must be able to successfully pass the Basic Windows Skill Assessment at 80% or higher rating within 30 days of employment
Good communication, organization, and interpersonal skills
Good working relationships with colleagues, subordinates, and superiors
Develops, conducts, and facilitates research protocols
Supports investigators in writing study protocols
Performs participant screening, enrollment, study activities, and communication
Maintains equipment and supply resources for research studies
Obtains informed consent by following policy, procedure, and regulatory requirements
Schedules study-specific visits in conjunction with ancillary departments
Completes data management activities
Assists in the development and completion of source documents and case report forms
Completes data entry and ensures data integrity
Supports statistical services needs
Directs patient interaction to conduct research protocols
Completes research-only testing as required and applicable per study and system requirements, including electrocardiograms
Performs phlebotomy if trained to do so
Completes documentation as needed within the medical record
Monitors compliance throughout all study activities and engages compliance oversight as needed
Participates in education activities to support specific research activities and primary role at Children’s Healthcare of Atlanta
Maintains all licensure, certification, and system education requirements for role
Participates in educational activities related to study needs for study staff, investigator team, and patient care staff
Participates in departmental policy and quality projects
Manages all regulatory processes related to clinical research activities
Completes Institutional Review Board preparation, submission, modifications, reporting, and termination activities
Maintains all regulatory documents
Participates in sponsor correspondence, monitoring, and study meetings
Facilitates grants, contracts, and financial tasks for research and clinical trials
Supports Principal Investigator in study budgeting, sponsor interactions, routing, feasibility assessments, account management, and reconciliation

196

Senior Research Coordinator Resume Examples & Samples

3 years of experience in clinical research with knowledge about the conduct of clinical trials, research principles, and methodologies/study design
Basic statistics
Self-motivated from a performance and professional development standpoint
Commitment to the lab’s and Children's Healthcare of Atlanta's missions, goals, and values
Broad knowledge of federal regulations and regulatory requirements for conducting research with the ability to mentor
Strives for good working relationships with colleagues, subordinates, and superiors
Develops, conducts, and facilitates research protocol at an expert level
Provides substantial support for investigators in writing study protocols
Leads participant screening, enrollment, study activities, and communication
Coordinates study visits and procedures, including specimen acquisition, transport, documentation, and shipment
Monitors process for services
Acquires equipment and supply resources for research studies
Provides leadership for data management activities
Develops and evaluates source and case report form tools
Manages data entry, ensures data integrity, supports statistical services needs, and collaborates with manager to assess data management needs
Provides leadership for direct patient care interaction
Completes research-only testing as required and applicable per-study and system requirements, including electrocardiograms
Coordinates educational activities related to study needs for study staff, investigator team, and patient care staff
Initiates departmental policy and quality projects
Provides leadership and training related to all regulatory processes related to clinical research activities
Ensures Institutional Review Board preparation, submission, modifications, reporting, and termination activities
Structures the maintenance of all regulatory documents
Leads others in sponsor correspondence, monitoring, and study meetings
Guides interdepartmental auditing of regulator practices
Independently provides services for investigators in study budgeting, sponsor interactions, routing, feasibility assessments, account management, and reconciliation
Serves as a collaborator and key contact for key business partners, including Emory, Georgia Tech, and University of Georgia
Works collaboratively with manager to monitor metrics

197

Research Coordinator Resume Examples & Samples

Knowledge in collecting heights, weights, behavioral, and physical activity data helpful
Ability to motivate parents and children to participate in the study and recommend it to family and friends
Fast learner, great organizational skills, resourceful, and capable of multi- tasking
Bilingual in Spanish and English is required
Must have a car or other ways of getting to community study sites around Houston, Texas, as work is performed at the Children’s Nutrition Research Center (CNRC) and various neighborhoods in Houston. Flexibility and adaptability in work schedule and carrying out job duties, including willingness to work some evening and weekend hours
Must be able to lift and move required assessment and physical activity equipment and materials. Ability to demonstrate fundamental movement skills and exercise to fathers and children

198

Senior Clinical Research Coordinator Resume Examples & Samples

In collaboration with the Cardiovascular Institute physicians, obtains source documents (i.e. medical record documentation) as needed
Obtains consent and registers research participants with study sponsor (e.g. industry, NIH, etc.)
Maintains research record (e.g. patient consent, eligibility, case report forms (CRF), registration confirmation, corresponding source documents, etc.) for all patients enrolled in clinical trials
In collaboration with the physicians, completes and submits Serious/Unexpected Adverse Event Form for all internal and multicenter serious/unexpected adverse events as required by study sponsors, federal requirements and institutional guidelines
Actively participates in weekly Cardiovascular Institute meetings and conference calls (as applicable)
Maintains regulatory documents of epidemiology studies and clinical research databases
Communicates effectively with staff and outside agencies, and assists in the promotion of teamwork

200

Abcd Research Coordinator Resume Examples & Samples

Theoretical knowledge of psychiatry, psychology, or related field, and previous research experience in the related field
Bi-lingual, fluency in English and Spanish
Proficiency in using database software including Microsoft Office (Word, Access, Excel, and Power Point). Familiarity with using iPads and apps including Pearson/Q-Interactive, and NIH ToolBox. Experience using content collaboration software including Confluence and DropBox. Working knowledge of REDCap and E-Prime
Experience performing research duties in a clinical research environment and coordinating research studies. Experience with following a standardized multi-site Spanish and English research protocol in order to screen patients for eligibility, initiate study procedures, and collect data
Knowledge of MRI and Mock Scan procedures and MRI safety. Experience screening youth MRI subjects via the parent/legal guardian for MRI contraindications. Ability to maintain current MRI Safety Training and Certification through UCSD Keck Center for functional MRI and Mock Scan Training and Certification
Working knowledge of longitudinal research design and methodology and DSM V criteria
Experience administering detailed clinical interviews to youth and their parent/guardian including administering KSADS 5, demographic, mental health history, and experience asking minors about and documenting lifetime history of substance use
Knowledge of or experience in collecting biological specimens including saliva, hair, and urine samples according to a standardized protocol and following universal precautions
Understanding of IRB and NIH annual and unexpected reporting including enrollment, withdrawals, adverse events, and protocol deviations
Excellent planning and organizational skills and ability to work in a changing, multiple-demand setting in order to prioritize a large volume of work and meet deadlines efficiently and accurately
Bachelor's degree in psychology or social sciences

201

Research Coordinator Resume Examples & Samples

Background in nutrition, health science or related field
Fluency (spoken and written) in English
Requires meticulous attention to detail
General computer skills including working knowledge of Microsoft Office, and the ability to learn new software, systems, databases
Must be self-sufficient and able to identify problems and solve them
Able to work collaboratively in a small team

202

Senior Clinical Research Coordinator Resume Examples & Samples

Master’s Degree in a relevant health care field is required; plus two (2) or three (3) years of clinical research experience
Applicants possessing an RN or LPN license may substitute equivalent related experience such as clinical or clinical research experience
Equivalent experience, education and/or training may be substituted for the education requirements
Solid knowledge of computer software programs such as Excel®, Word®, and/or PPT
The ideal candidate will be detail oriented, have excellent organizational, communication and interpersonal skills, holds self accountable to high standards of professional excellence, be able to maximize resources and be resourceful, seeks and accepts personal and professional responsibility on a continued basis

203

Research Coordinator Resume Examples & Samples

Bachelor's Degree. Significant experience in research coordination can be substituted for education
Minimum one year experience in related field
Basic knowledge of FDA research policies, other applicable federal regulations and/or GCP guidelines
Well-versed in medical and scientific terminology
Familiar with medical records departments and information

204

Seasonal Background Check Research Coordinator Resume Examples & Samples

Conduct phone evaluations with candidates regarding information submitted on employment applications; Information would be including, but not limited to, criminal conviction history
Conduct phone evaluations with a high degree of accuracy, confidentiality and integrity
Maintain candidate focus to gather all information within the designated timeframe
Evaluate candidate responses to make an appropriate business decision while remaining compliant with all Federal, State, Local laws and EEOC and other agencies guidance’s relating to Employment background check policies
Prior Human Resources experience a plus, but not required
Ability to read, write and interpret instructional documents such as reports and procedure manuals

205

Research Coordinator Resume Examples & Samples

Excellent computer skills with knowledge of Access, MS Word, Excel, Outlook, PowerPoint
Meticulous organizational skills and proven ability to multi-task and work independently and
Demonstrated problem-solving ability and attention to detail while working in a fast-paced, deadline

206

Internship Research Coordinator Resume Examples & Samples

Experience with prospect and/or employer research
Experience working with CRM tools and systems
Experience managing data, including collection, entry, analysis, and reporting
Technical proficiency including Excel/mail merge/databases
Demonstrated skill with report writing and presentation of data
Demonstrated ability to provide high-quality customer service to staff, faculty, students & external partners and to collaborate across departments in a complex organization
Demonstrated commitment to principles of community and diversity, and the ability and desire to effectively and consistently relate to a diverse student population
Advising or mentoring experience is a plus

207

OPS Research Coordinator Resume Examples & Samples

Maintain participant records including informed consent and experimental procedures
Manage international media distribution via website monitoring and maintenance
Serve as liaison between university personnel and laboratory operations
Assist in manuscript preparation and submission
Assist with participant recruitment and scheduling
Assist in updating and maintaining laboratory website
Assist with planning and preparing visits from international scholars
Coordinate schedules and duties of laboratory research assistants and other personnel
Work with Center director and associated faculty on research-related needs

208

Research Coordinator Resume Examples & Samples

Manage the day-to-day operations of the research projects with investigators, consultants, data managers, study coordinators, outreach workers, and clinical staff
Coordinate all apects of the research projects with the study team
Hire, Train, and supervise 3 study coordinators, 1-2 outreach workers, student researchers, and volunteer staff
Work with the Principal Investigator (PI) to develop and update study protocols, including the development of new measures
Manage all Institutional Review Board (IRB)-related activities
Create regular reports for the IRB, funders (NIH and others) and PI
Coordinate meetings with study partners and represent study at clinical site meetings
Work with PI to develop recruitment strategies and manage tracking database; prepare weekly (and more frequent if needed) reports to PI about recruitment/tracking
Partner with IT/EPIC team and data programmers to modify and maintain study databases
Securely manage and maintain study data base
Perform regular audits to ensure that collected data are complete and accurate, and research protocols are being followed
Conduct research site visits to ensure that intervention is implemented as per protocol; maintain close communication with clinic champions along with study coordinators, conduct and supervise participant computer-assisted interviews
Extract and examine medical records
Assist in data analysis, drafting reports, preparing conference abstracts and presentations related to the project (e.g. posters, PowerPoint presentations)
Maintain and order study-related supplies
Maintain records of study incentives and travel reimbursements; facilitate other study-related financial transaction
Supervise, coordinate, and conduct data collection, data entry, and data management
Lead weekly project meetings
Supervise participant recruitment, tracking, and follow-up
Participate in disseminating study findings
Assist with preparationa dn writing of grant proposals
Troubleshoot study-related problems
Collaborate with Divisions Administrative staff to ensure execution of program budgets, subcontracts, consultant contracts and grant proposal submissions
Travel to clinical and research sites in the Bronx to oversee all study-related activities and facilitate participant recruitment and follow-up
Minimum Bachelor's degree required. Master's degree in Public Health, clinical epidemiology, or related field preferred
At least 3-5 years of experience managing research projects and staff
At least 3-5 years of experience collecting data for research (e.g. recruitment, conducting interview, extracting medical records and data analysis)
At least 2 years of experience working with a similar population
Advanced working knowledge of Microsoft Word, ACCESSm EXCEL, RedCap and SPSS (or SAS, STATA)
Ability to manage multiple priorities and projects while working as part of a geographically disbursed team, work with minimal supervision, and adhere to study protocol
Excellent interpersonal, organizational, and communication skills
Able to write scientific documents
Flexibility and willingness to work evenings and weekends are necessary
Fluency in English and Spanish required

209

Research Coordinator Resume Examples & Samples

Maintains and manages research databases of study participants, responsible for ensuring accuracy of data collection, data entry and adherence to established research guidelines
Conducts research interviews, screens subjects for participation in various research studies
Prepares Institutional Review Board applications and maintains regulatory documents for Institutional Review Board compliance for various research projects
Recruits research subjects and coordinates research visits. Meets with the participant and parent and/or guardian of the research participant to review and obtain consent for participation
May perform educational, developmental, or other forms of testing as required with research participants
Analyzes behavioral data, generates reports and builds queries
Assists with processing and analyzing neuroimaging data
Assists with planning and developing survey instruments
Participates in development of grant proposals and manuscript preparation including, but not limited to, conducting literature searches, performing data analyses, and assisting in the writing of manuscripts and grants
Orients students, research assistants and authorized visitors to the department and research protocols
Designs and conducts research experiments under the direction of the Associate Professor
Schedules and participates in research meetings
Must have 2 years’ experience coordinating investigator-initiated research protocols required
Some professional experience in a pediatric setting preferred

210

Research Coordinator Resume Examples & Samples

Collaborates with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols. Monitors and reports on progress of projects
Assists with the recruitment, selection, scheduling, and monitoring of research project participants. Manages the handling of adverse events, compliance and other participant-related issues
Collaborates to ensure compliance with applicable regulations and standards. Assists with responding to and preparing for audits
Manages clinical and regulatory compliance of the protocol including administration of study drug/device, adverse events/safety issues, medication interactions. May be required to respond to call

211

Senior Research Coordinator Resume Examples & Samples

Performs patient/family education about clinical trials as well as the research protocols. Ensures research needs are met at all family meetings (discuss progress of treatment, changes in therapy)
Acts as liaison between patient and physician concerning problems, adverse reactions, and other patient care issues, that may be related to the study
Follows-up with patients during each clinic visit to answer questions and assess for toxicities
Five years of relevant experience in a research or health care setting with Bachelor's degree or nine years of relevant experience in a research or health care setting without a Bachelor's degree

212

Research Coordinator Resume Examples & Samples

A minimum of 3 years of clinical operations experience, with increasing levels of responsibility. preferred to have clinical trials program management experience in Academia, Pharmaceutical, Biotechnology, Medical Device and/or CRO industry
Must have prior experience managing a clinical trial portfolio or large scale clinical trial program globally and be able to demonstrate a proven track record of successfully leading cross-functional projects in a global environment
Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH/Good Clinical Practices regarding drug development phases, clinical research and data management methods
Therapeutic experience in infectious diseases preferred
Experience in early phase trials (Phase I-II) and First-In-Man trials is preferred
Ability to travel domestically and internationally is required

213

Research Coordinator Resume Examples & Samples

Three Years of relevant experience in a research or health care setting without a Bachelor degree. No experience required if candidate has a Bachelor degree in a related field
Excellent people skills
Complete all required training to conduct clinical research

214

Research Coordinator Supervisor Resume Examples & Samples

Supervises, hires, trains, disciplines and evaluates the performance of staff. Ensures performance appraisals are completed in a timely fashion
Provides technical and functional expertise in the area of Research studies. Recommends appropriate implementation plan. Monitors study routine to ensure progress of studies and reports to PI. Oversees compliance with regulatory and granting agencies
Makes recommendations for program enhancements, performance improvement, and "best practices."
Maintains comprehensive study lists for departmental information. Maintains cooperative relations with drug companies and other research centers for information on new research interests
Collaborates with PI and acts as a liaison between the Food and Drug Administration and drug companies on related issues. Adheres to and trains research staff on Good Clinical Practice, and regulatory and grant agency requirements. Keeps investigator informed of protocol changes or developments
Liaises with agencies including: IRB, OCG, pharmaceutical companies, laboratories, and equipment and supply companies as needed
Responsible for coordination of the day-to-day activities of the designated study or group of studies in clinical based research; ensures appropriate screening and oversees recruitment of subjects, implements study procedures, supervises the scheduling of experiments and the collection, processing and analysis of data
Ensures the safety and comfort of patients being evaluated. Supervises the scheduling of patients for clinical and biological evaluations; sets up educational workshops for patients and families; and provides on-call coverage for patient concerns/complications
Administers scores and evaluates assessments as assigned and as related to study protocol. Collects data, confers with PI and forwards results to sponsor (internal or external)
Interfaces with the Office of Grants and Contracts (OGC) and Institutional Review Board (IRB). Organizes all phases of grant process for submission to funding agencies as necessary
Bachelor's Degree, in a field of Science, Behavioral Science or related field, required
Minimum of three (3) years progressively responsible related work experience, including leadership, to ensure working knowledge of research methods and analysis
IRB Human Subject Protection training, required
Certification in venipuncture, electrocardiogram and vital signs, as needed per study protocols, required
Certified as a Clinical Research Professional, preferred
Excellent written and oral communication skills, required

215

Research Coordinator Resume Examples & Samples

Collaborate with investigators in the design, development, and documentation of data forms, questionnaires, and other survey materials
Responsible for aspects of the development of research recommendations and the design of research projects
Participate in the grant, manuscript, and Institutional Review Board process
Develop overall research plan for conducting surveys in the community
Conduct in-person or telephonic field research
Monitor selection and randomization process of study participants
Coordinate data collection of study participants, complete case report forms, and develop and maintain spreadsheets
Collect and maintain questionnaires and other data forms from study participants
Perform literature searches and write detailed written summaries of the findings
Collaborate with other project leaders on data presentation, interpretation and writing of scientific reports
Develop and maintain computerized data files for all data to be collected
May assist with budget /operational aspect of grant and contract proposals
Prepare summary reports and ongoing project evaluations for investigators
May help recruit, select, supervise and direct the activities of data collection employees and Research Technicians
Conduct quality control check on field data collection system
Collaborate with other research sites to insure consistency between research sites and accuracy of documentation
Bachelor’s degree in the sciences, health care, or equivalent experience
1 year of related experience
Excellent organization, analytical, and interpersonal skills required

216

Research Coordinator Resume Examples & Samples

Provide support to projects through implementation of work plans, and preparation of deliverables. Assist in the documentation of project writing, preparation of material for project meetings and IRB submissions, summary reports, ongoing project evaluations, and coordinate arrangements applicable to assigned projects such as interview arrangements, etc
Administratively responsible for the clinical aspects of patient study subjects and testing
Participate in preparing project-specific data collection efforts including surveys, interviews, focus groups involving patients, state agency personnel and other key informants. Record and analyze pertinent data. Evaluate and update data in relation to protocol
Design and execute protocols and experiments, modify protocols as needed, and may be responsible for own research project
Oversee development of data collection instruments, survey tools and interview guides, perform and oversee data collection, management and analysis as necessary
Assist in writing the text of scientific publications and grants. Review literature
Assist in design, development and implementation of research endeavors for multiple principal investigators
Assist with the budget/operational aspects of the revenue and expense accounts. Compile expenses for fiscal reports and grant budgets. Assist grant accounting with grant reporting requirements
Responsible for maintaining all regulatory paperwork from study initiation, continuation, and termination (includes application for IRB, informed consents, HIPAA Authorization, etc.)
May help recruit, select, supervise and direct the activities of data collection employees, Research Technicians, and Research Coordinators
Comply with all safety and infection control standards appropriate to this position
Responsible for the inventory of research related supplies
3 years of related experience
Demonstratedknowledge of federal requirements for the conduct of clinical trials
Experience in using computer based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)

217

Senior Clinical Research Coordinator Resume Examples & Samples

Develop study protocols and data collection forms in collaboration with study investigators
Develop patient navigation intervention with investigators
Provide individual navigation to patients participating in the program
Work with senior level staff at health center sites to negotiate/implement/monitor research protocols
Train clinical research staff on the implementation of the intervention protocols, as well as the collection and documentation of data
Oversee adherence to project timelines
Coordinate Institutional Review Board (IRB) applications, continuing reviews, amendments, and files adverse events with the IRB
Plans, performs, and designs statistical analysis of findings
Set agendas for study team meetings
Serves as resource for patients during the course of the intervention
Performs reference searches in print and electronic media
Responsible for quality control and developing systems for QA/QC
Review data for quality assurance, descriptive statistics and manuscripts, as required
Assist with writing reports and manuscripts detailing research findings
Develops study budgets and assumes grant management responsibilities
High level time management and organizational skills
Ability to prepare and monitor budgets
Knowledge of current and developing research trends
Ability to meet the requirements of funding sources
Sound interpersonal skills and the ability to supervise others
Ability to identify problems and develop solutions
Ability to operate independently in a community health center setting and with good judgment
Proficiency of various software packages, including Microsoft Office, and other desktop tools
Ability to meet deadlines and work within budgets
Ability to compile data, analyze information, and produce reports
Bilingual in English and Spanish, preferred

218

Senior Clinical Research Coordinator Resume Examples & Samples

Nurses with 2 years of nursing experience may be considered for this position. The title and salary range of the position may vary depending on education level and any years of relevant research background**
Demonstrates a passion for developing others, enthusiastically and expertly precepts new hires during the orientation process, and serves continuously as a mentor. Analyzes clinical and behavioral situations, identifying learning opportunities to improve patient care and clinical research practices. Takes responsibility for identifying his or her ongoing professional development needs and independently seeks resources and opportunities to meet those needs, such as through membership in nursing, oncology, or research organizations. Regularly seeks feedback on performance and applies continuous professional improvement
Demonstrates productive working relationships internally and externally by taking accountability for actions, enthusiasm, motivation, commitment to patients and colleagues. Demonstrates an understanding of cultural differences and holds peers accountable for healthy relationships and maintains a conscious balance between work and personal life. Models safe work hours, time management and healthy lifestyle. AGE SPECIFIC COMPETENCY: The individual must be able to identify the patient's particular needs regarding age, education level, literacy and the presence of any language barriers so that all clinical research related instructions can be adapted to the patient's needs. This is particular important regarding the informed consent process. Must also be aware of the various institutional resources to facilitate this process. Note: The above statements are intended to describe the general nature and level of work being performed by people assigned this job. They are not exhaustive lists of all duties, responsibilities, knowledge, skills, abilities and working conditions associated with the job
Identifies opportunities to improve research practices and patient satisfaction by serving or leading teams as a change agent to launch innovations in patient care/satisfaction, clinical research, or supporting a healthy workforce. Actively participates in department or unit-specific quality improvement efforts. Identifies opportunity for quality improvement to colleagues and management
Provides an ongoing annual professional contribution: Ensures research documentation is comprehensive and facilitates protocol compliance; communication among colleagues; good clinical research practice; and patient safety. Utilizes a variety of strategies to enhance recruitment while being mindful of the needs of diverse patient populations and variables (fiscal and contractual) that affect clinical research. Practices solid communication skills, and is able to articulate and translate pertinent information. Creates a caring and compassionate experience by building healthy relationships with patients, families and colleagues
Serves as a role model of professional nursing practice as demonstrated by adherence to ethical practices during the conduct of clinical trials to protect the rights and well-being of patients and the collection of quality data. Consistently provides appropriate feedback to all members of the research team; participates in the peer review process; and utilizes multiple communication methods to facilitate the effective conduct of clinical trials. Demonstrates highly developed assessment and analytical skills within the context of clinical research by ensuring complete and accurate documentation to validate the integrity of trial conduct. Ensures the patient is initially and subsequently appropriately informed of protocol related/required procedures, expectations, and responsibilities as demonstrated by the documentation process of the Informed Consent
Minimum 2 years of nursing experience required
Minimum 2 years of research experience preferred, or required for Senior level
Annual completion of a VP approved professional contribution required for Senior level
Special Skills and Abilities Required Solid/Strong/Good or higher on most recent performance evaluation and maintain in practice Leadership abilities
Excellent role model

219

Senior Research Coordinator Resume Examples & Samples

Microsoft Office, ability to work with time-sensitive projects and write standard documents
Must be well organized with a keen attention to detail and able to multi-task
Must have excellent communication skills (both written and verbal) and the ability to analyze data/write/present
Spreadsheet, statistical analysis and data entry experience required as well as good customer service and patient care skills
Science and biology knowledge preferred
Patience and good customer service skills are critical as the patient population includes infants and children
Experience working with and troubleshooting computers preferred

220

Senior Clinical Research Coordinator Resume Examples & Samples

Assigns and oversees Assistant Clinical Research Coordinator duties on the assigned project
Responsible for monitoring volunteers’ compliance throughout the trial. Addresses day-to-day volunteer or study issues and escalates as appropriate
Prepares for and participates in sponsor/monitor/QA audits
Provides accurate and timely project status updates to Project Managers and sponsors
Ensures ongoing and timely communication with the Assistant Clinical Research Coordinator (ACRC) and other study team members
Actively participates or takes the lead with own team and others in process improvements, SOPs creation and/or revision, internal and external meetings and other team or company-related initiatives and goals
Serves as lead and main team liaison for common external vendors (local lab) and maintains and tracks these vendors
With or in the absence of management, provides guidance on study or team-related issues; supervises and provides feedback on clinic operations as required
Identifies training needs, establishes training materials and provides training within the team and others
With management and as required, assists in hiring and training of new staff and performance management of staff

221

Oncology Clinical Research Coordinator Resume Examples & Samples

Bachelor’s Degree in a relevant science or a related field (e.g. public health, health care administration) required
A minimum of one to three (1-3) years of research related experience, strong research specific knowledge base, solid knowledge of computer software programs such as Excel®, Word®, and/or Access®
The ideal candidate will be detail orientated, have excellent organizational, communication and interpersonal skills, hold self-accountable to high standards of professional excellence, be able to maximize resources and be resourceful, seeks and accepts personal and professional responsibility on a continued basis
Able to function independently and adjust hours to meet job demands
Association of Clinical Research Professional (ACRP) certification as a Clinical Research Coordinator (CRC) or Clinical Research Associate (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP) is preferred

222

Research Coordinator Resume Examples & Samples

Work with internal and external departments to understand research objectives and execute that plan as quickly and efficiently as possible
Run and maintain large scale count and quota tracking sheets
Assist with the development of tab plans as well as efficient visual ways of understanding the data
Run data requests using Decipher, STATA, R, or Survey/Reporter
Weekend, non-traditional business hours and some travel maybe required
BS/BA in Business, Marketing, Market Research or related field
2 years’ experience in market research, consumer insights, brand management and/or strategy
Familiarity with quantitative research
Able to work autonomously
Possess the ability to identify gaps in process and documentation and take the lead on updating documentation
Ability to work on demanding projects with very tight timelines

223

Oncology Clinical Research Coordinator Resume Examples & Samples

Bachelor’s Degree in a relevant science or a related field (e.g. public health, healthcare administration)
Five (5) years of research related experience, strong research specific knowledge base, solid knowledge of computer software programs such as Excel®, Word®, and/or Access® required
Association of Clinical Research Professional (ACRP) certification as a Clinical Research Coordinator (CRC) or Clinical Research Associate (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP),is required
The ideal candidate will be detail orientated, have excellent organizational, communication and interpersonal skills, hold self accountable to high standards of professional excellence, be able to maximize resources and be resourceful, and seeks and accepts personal and professional responsibility on a continued basis
Equivalent experience, and/or training may be substituted for the education requirements

224

Research Coordinator Resume Examples & Samples

Coordinates day to day activities of research protocols which include screening, enrollment, and monitoring of research participants
Ensures accurate data collection, documentation, organization and safety of research participants
Interview, screen and recruit patients for study
Explains process and procedures to educate participant regarding the research study
Collects patient information
Process, document and enter information into a database
May perform Venipuncture (blood draws), EKGs/ECG’s and obtain vital signs on study participants
May collect, process, ship, and maintain paperwork for blood and/or biological specimens according to procedures outlined in study protocol
Employees may be required to receive on the job training of phlebotomy and EKGs/ECGs prior to performing on study participants
Maintains records and regulatory documents and records for research studies
Schedule research participant for tests and procedures, such as laboratory tests, x-rays, and other studies specific for the research protocol
Perform other job duties as assigned

225

Assistant Clinical Research Coordinator Resume Examples & Samples

HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities
Proficiency with Microsoft Word, PowerPoint, and Windows
Excellent analytical and problem-solving skills
Ability to work effectively in a fast-paced, team-based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects
Ability to establish cooperative working relationships with patients, co-workers, & physicians
Demonstrated proficiency with medical terminology

226

Assistant Clinical Research Coordinator Resume Examples & Samples

High School graduation or a General Education Diploma; and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities
Detail oriented, self-motivated and a record of exceptional performance meeting multiple deadlines for concurrent projects
Knowledge performing statistical analysis obtained through course study
Ability to analyze data using Matlab and other statistical software

227

Assistant Clinical Research Coordinator Resume Examples & Samples

HS degree or equivalent and six months to one year of related work experience
Proficiency with Microsoft Word, Excel, PowerPoint, and Windows
Demonstrated skills to successfully perform the assigned duties and responsibilities
Ability to exercise judgment and initiative
Must be detail oriented, self-motivated and able to meet multiple deadlines for projects
Ability to speak and write English
Statistical analysis background

228

Assistant Clinical Research Coordinator Resume Examples & Samples

Fluency in Cantonese language, verbally and in reading
Proficiency with Outlook, Excel, and Word, and experience with in database utilization
Ability to work with geriatric and cognitively impaired individuals
Fluency in Mandarin language (in addition to Cantonese, which is required)
Coursework in human or cognitive neuroscience
Experience administering cognitive tests

229

Assistant Clinical Research Coordinator Resume Examples & Samples

Working experience in Microsoft Word, Excel, PowerPoint, and experience with a statistical program such as STATA or SPSS
Abilities in conducting scientific literature searches and written summaries
Familiarity with scientific presentation and abilities in preparation of slides and reports
Ability to work respectfully with diverse communities to recruit young adult tobacco users for research
Outstanding communication skills both internal and external to the study team
Ability to identify problems, troubleshoot and propose solutions to the team
Demonstrated strong administrative and organizational skills

230

Assistant Clinical Research Coordinator Resume Examples & Samples

Bilingual in English and Cantonese and/or Mandarin
Must be comfortable, sensitive and operate within confidentiality standards with topics related to health and cancer
Travel within San Francisco required
Minimum one year prior experience working in healthcare related phone survey administration
Experience working in REDCap

231

Senior Clinical Research Coordinator Resume Examples & Samples

High school graduation or General Equivalency Diploma and three or more years of related work experience; or an equivalent combination of education and experience
In-depth knowledge of clinical research contracts and grants, clinical trials, protocols, FDA regulations, and complex visit structures
Financial analysis skills; demonstrated skills in preparing and presenting financial and quantitative analyses, including financial projections and budgets
Fluency in spreadsheet software; ability to develop and manage complex spreadsheets independently
Project management skills to oversee the administrative operations of the clinical trials program; knowledge of strategies for recruiting human subjects
Exceptional analytical skills to evaluate the importance and urgency of problems; excellent demonstrated interpersonal, verbal and written communication skills
Ability to analyze complex and non-routine issues requiring innovative solutions
Ability to operate effectively in a changing organizational and technological environment
Ability to assess and respond to audit risk; ability to develop project plans/schedules and motivate team to meet deadlines
Ability to interpret and apply policies and regulations
Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals (within one year of hire)
Experience in risk management regarding study subjects, federal and non-federal sponsors and regulatory authorities
Experience with contract generation and subcontracting, preferably at UCSF
Experience using database software, such as MS Access or FileMaker Pro

232

Assistant Clinical Research Coordinator Resume Examples & Samples

Knowledge of patient confidentiality and HIPPA regulations (electronic and hard copy medical records, patient charts, communication, etc.)
Experience working with patients in a health care setting
Bachelor or Associate degree in health related field
Phlebotomy license (CPT1)
Bilingual (fluent in Spanish and English)
Ability to abstract data from electronic medical records (EPIC)

233

Assistant Clinical Research Coordinator Resume Examples & Samples

Fluency in English and Spanish Languages (written and spoken)
Proficiency in Microsoft Word, PowerPoint, and Windows
Bachelor’s or higher degree in Psychology, Neuroscience, Cognitive Science, or Biology
Experience and interest in elderly populations
Knowledge of CHR/IRB policy and procedure
Proficiency in data analyses software (SPSS, Stata, MatLab)
Willingness to perform administrative duties

234

Senior Clinical Research Coordinator Resume Examples & Samples

High school graduation or General Education Diploma and three or more years of related work experience; or an equivalent combination of education and experience
Significant project and clinical trial management experience or progressively responsible experience in a related position including regulatory and compliance responsibilities
Demonstrated ability to develop recruitment strategies in complex environments and differing patient pools, independently identifying recruitment leads, implementing new strategies, and continually adjusting strategies to meet current recruitment goals
Current certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals or ability to obtain within one year after hire
Good Clinical Practices (GCP) training
Current Basic Life Support Training (CPR) certificate
Prior experience in investigational drug clinical research (i.e. FDA clinical trials)
Fluency in spreadsheet software; ability to develop complex spreadsheets independently; demonstrated skills in audit preparation, execution, and follow-up
Experience in risk management regarding study subjects, federal and non-federal sponsors and regulating bodies
Experience with grant application procedures, personnel documentation, contract generation and subcontracting, preferably at UCSF

235

Research Coordinator Resume Examples & Samples

Plan, implement and monitor participant recruitment and retention procedures
Screen and interview study participants
Maintain case report forms, charts and documentation
Perform procedures as needed
Assists Division staff as needed
Job related travel as necessary
Writes status reports of current studies and updates departmental faculty on quarterly bases
Maintains database as requested by staff
Assists residents and fellows in research projects and the acquisition of data
Develop databases for the departmental staff
Assist staff in acquisition of IRB Applications
Maintains database on active IRB Studies for the department
Performs literature reviews as requested by staff
Maintains regulatory compliance and regulatory binders
Assists resident’s fellows and faculty in initial manuscript writing
Collaborate with study personnel in the strategic planning of future external funding grants
Develops research protocols that clearly describe research objectives and procedures necessary to test the hypotheses of the research project
Develop research designs, data collection methods and strategies for data management
Design, create and revise research instruments as necessary to ensure quality data that correlates with research objectives
Coordinates multiple data collection efforts for one or more research projects which may include other collaborating agencies or institutions
Consult with co-investigators on appropriate management of participant problems and concerns
Develop and manage interim reports for principal investigators, industry sponsors and institutional review board to ensure that each project is moving toward timely completion
Ensure that projects are executed successfully and completed within time frames to meet research objectives
Assists in preparation of all documents related to the informed consent process
Assists Principal Investigator in preparation and submission of informed consent documents to the appropriate departments
2-5 years of nursing experience is preferred

236

Lead Clinical Research Coordinator Resume Examples & Samples

AA or BS degree in biological or clinical sciences
Previous hospital experience, experience abstracting or coding information from patient medical records
Laboratory skills for the safe operation of standard clinical centrifuge, separation of blood components, skilled handling of biohazardous material, pipeting, use of dry ice and liquid nitrogen for freezing and/or storing clinical samples
Effective oral and written communication skills
Skilled at chart review and abstracting data from patient charts
Skilled in finding and abstracting specific, required information from complex documents (e.g. Patient records, study protocols, etc.)
Competent in MS-Word and MS-Excel applications
Interpersonal skills necessary to work effectively with physicians, patients, nursing and ancillary staff in a variety of contact settings
Appropriate knowledge of anatomy, physiology, disease process and standard treatment protocols
Knowledge of Good Clinical Practice and ICH guidelines as adopted by the FDA
Working knowledge of Hospital research policies and procedures, HIPAA guidelines, IRB’s, and FDA regulatory requirements for clinical studies
Demonstrated maturity and capacity to maintain confidential information
Demonstrated ability to complete assigned tasks accurately and timely with appropriate training and supervision
Ability to take direction and to establish priorities, to self-direct and work independently

237

Research Coordinator Resume Examples & Samples

Assists with planning and staffing of project operations based on proposed research activities and timelines. Coordinates aspects of sponsor initiated and investigator-initiated research studies including subject recruitment, data collection, scheduling of study-related activities and follow-up of enrolled subjects. Provides guidance and direction to investigators, research personnel, and subjects. Assists with training and demonstrating techniques or procedures to less experienced research coordinators
Assists in recruiting subjects for studies and determines eligibility based on study criteria. Coordinates study participant activities including recruitment, screening, orientation and correspondence. Schedules subject appointments, tests, and procedures coordinating with external providers as needed. Produces reports, correspondence and other materials, as needed or required
Has responsibility for data collection for research studies following established data collection and management procedures. Collects, records, enters and prepares data for analysis. Performs basic study analysis under the direction of the Principal Investigator. Collects pertinent information from study participants through interviews, administration of tests or surveys or questionnaires, medical records review, or other collection procedures

238

Market Research Coordinator Resume Examples & Samples

Manage and optimize function space to ensure effective use of space
Analyze historical demand and create best practice scenarios to measure business opportunities against ideal date patterns, rooms to space ratio, food and beverage contributions and total revenue
Track and audit all space assignments on a daily basis
Maintain the Group Rooms Control Log (GRC)
Daily logging and distribution of definite and tentative bookings, cancellations, and revaluation’s
Generate the Weekly Sales Activity Report
Preparation and typing of the Advanced Sales Report/Director of Marketing Letter at the end of each month (to be in Corporate Office by the 3rd working day of the month)
Prepare and distribute monthly forecast
Generate 30-60-90 day forecasts as needed by the Director of Marketing and Director of Sales
Preparation and typing of Monthly Inventory Growth Analysis
Responsible for the OSCAR Program and it's parameters
Maintain a Kill file for Lead information
Maintain a Lost Business file
Distribution of Housing Pick-up Reports, Firm Rate Commitment Forms, and convention memoranda from Convention and Visitors Bureau
Aid the Director of Marketing and Director of Sales in monitoring the KRA benchmarks
Responsible to maintain monthly recap with reservations to insure GRC blocks is the same as Reservation blocks
Attend Weekly Sales Meetings
Assist Director of Marketing with coordination of special promotion mailings
Assist the office manager and the Director of Marketing in special projects
Bachelor’s Degree in Business or Hospitality Management is preferred

239

Assistant Clinical Research Coordinator Resume Examples & Samples

High School graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities
Ability to work effectively in a fast-paced, team-based environment; ability to prioritize tasks and meet multiple deadlines on concurrent projects
Ability to establish cooperative working relationships with participants and co-workers
Demonstrated proficiency with research terminology
Experience working with participants in a research setting
Proficiency with statistical analysis software

240

Research Coordinator Resume Examples & Samples

Participate in preparation and writing of manuscripts, technical reports, formal presentations, and grant applications. Duties include preparing charts and tables, composing initial drafts, organizing and maintaining citations, doing data checks, and formatting documents following journal or grant guidelines
Assists with data collection and data entry of surveys and qualitative interviews. Assists in the coordination of project staff activities related to data collection. Assists PI and Faculty leadership in the supervision of data collection to ensure the project remains within the approved IRB protocol, as well as within timeline and budget concerns
Searches and organizes scientific literature using relevant databases and other sources (e.g., Medline and CSA databases); maintains bibliographical citation data using an appropriate software such as Endnote; prepares written summaries of literature
Master’s Degree with at least two years of experience in health-related research or quality evaluation
Attention to detail, particularly with regard to data accuracy and integrity
Strong computer skills (MS Office – including Word, Excel, PowerPoint, and Access)
Good working knowledge of data analysis software (e.g., SAS, SPSS or STATA)
Ability to handle protected health information and related human subject issues
Ability to travel to other locations within Florida for data collection and professional project meetings
Ability to interpret basic statistical results
Ability to work closely with PI and faculty to draft project proposals, manuscripts for publication in peer-review journals, and project reports
Ability to work independently, demonstrate initiative, and to collaborate with faculty and staff at multiple levels
Willingness to learn new skill sets and work in a cohesive team environment

241

Research Coordinator Resume Examples & Samples

Recruiting, screening, educating, and assisting potential study enrollees and their families throughout the length of the study
Obtaining informed consent
Scheduling research subjects’ appointments for tests and procedures
Responsibly handling and shipping biospecimens
Retrieving and submitting test results to appropriate party or data coordinating center
Entering study data from patients, families and medical records into a computerized database and/or on a case report form
Ensuring compliance with NIH and IRB regulations
Maintaining records and regulatory documents
Working effectively with a team of research coordinator to ensure appropriate and high-quality cross-coverage of different protocols
Participating in weekly project meetings
Helping meet study timelines as determined by the PI
Prefer fluent in Spanish and previous regulatory experience

242

AP Research Coordinator Resume Examples & Samples

Process payment approvals for utility, property tax, and loan invoices for all assigned associations, ensuring duplicates and other errors are corrected prior to check issuance
Team with property management to capture correct invoice information and to ensure processes are followed for timely payment of invoices to association vendors
Assist with ensuring proper workflows are established and maintained for routing of invoices through the approval process
Assist property management with proper coding of invoices to the general ledger
Troubleshoot issues in regards to invoices and payments
Provide training, guidance and support to system users in their information requirements, process management, and application knowledge; assist users on new processes and functions
Identify reoccurring errors and recommend training, documents and/or procedures to reduce errors
Research and respond to inquiries including, but not limited to, clarifying when an invoice will get paid, why an invoice was paid incorrectly and how to properly code an invoice
Research and resolve invoice issues related to unidentified properties, vendor issues, potential duplicate payments, image issues, missing invoices, missing payments, etc
Process the batching of approved invoices into the accounting system as well as resolve issues associated with this process
Support internal and external information requests
Resolve internal and external customer issues utilizing prompt, effective communication
Perform any range of special projects, tasks and other related duties as assigned
Three to five years of accounts payable experience
Must have strong computer proficiency and systems knowledge
Critical thinking, problem solving, good judgment and decision making abilities
Collaborative attitude and team player
Consistent professional demeanor
Work efficiently under pressure
Handle change in a positive manner
Reliable and discrete
Sitting at a desk for extended periods of time
Working at the computer throughout the day (keyboard and mouse use)
Ability to listen and focus for long periods of time
Ability to lift up to 30 lbs

243

Research Coordinator Resume Examples & Samples

2) Excellent English writing and speaking skills are required
3) Sufficient computer knowledge to interface with a variety of database, word processing, and scheduling
4) Good communication and interpersonal skills
5) Effectiveness in organizing tasks and setting priorities, multi-tasking, working efficiently with minimum oversight, interacting constructively with faculty and staff, and the ability to be adaptable, creative, and a quick learner
6) Flexible working hours including evenings and weekends is essential
3) Bilingual Spanish/English is a preferred

244

Mau-research Coordinator Resume Examples & Samples

Matches customer’s identified needs and criteria with available resources meeting minimum requirements of the department and expanding on this requirement to obtain personalised, confirmed, matched referrals or quick resources as appropriate
Creates, maintains and updates database with accurate information
Solves practical problems and interprets a variety of instructions furnished in written, oral, diagram, or schedule form
HSC and Diploma holder / Advanced Certificate in Management fields or Sociology or English or communication
Very good command of oral and written English and French
Very good telephone manner
Ability to work US/CA hours (from 17:00 pm to 02:00 am)

245

Mau-research Coordinator, Working Hours Resume Examples & Samples

Conducts independent research utilising an existing pre-populated database, as well as other resources such as research files, Internet, archives, collections, print directories and zip code books
Participates and contributes to achieve team objectives and to be customer focus
Develops and maintains a strong professional relationship with the community of providers
Strives for continual improvement against personal development objectives
Develops and maintains ability to work on multiple search requests simultaneously involving different resources and level of expertise
Meets deadlines or exceeds the minimum required amount of searches per day. Prioritise daily caseload to ensure that all work is completed on time
Evaluates articles and/or resources to determine which are most appropriate to meet customer needs
Ability to read, analyse and interpret professional journals, detailed reports and general business correspondence
At least 2 years of experience in customer facing environment
Computer literate (Word, Excel, Outlook, Internet Explorer)
Typing skills and experience in proofreading and editing will be an advantage
Articulate, reliable and self-motivating

246

Research Coordinator Resume Examples & Samples

Draft IRB documents for the research studies, including original applications, submission of amendments, and annual reviews
Prevent IRB problems from arising
Troubleshoot IRB problems if they do arise. Maintain close contact by phone and in person as necessary with IRB staff
Perform basic data analysis. Assemble datasets from different sources, and prepare reports summarizing progress and problems in ongoing research studies
Build and maintain electronic data capture systems utilizing RedCap
Perform other research duties as required
Ability to prioritize a high volume of work under potentially high pressure to meet deadlines
Familiarity with medical terminology
Prior experience reviewing medical records
Familiarity with Word, Excel, PowerPoint, and data management programs

247

Research Coordinator Resume Examples & Samples

Acquires subjects for psychophysical/eye tracking experiments
Plans, schedules and conducts research experiments
Collects, compiles and analyzes data
Documents and interprets results of experiments and reports to supervisor
May develop and modify computer programs
Oversees the maintenance of lab equipment and environment

248

Research Coordinator Resume Examples & Samples

Assists Clinical Research Manager with pre-study visits and feasibility assessments
Completes case-report forms and performs quality assurance checks on all data (in coordination with the Q/QC Manager)
Coordinates regulatory and IRB interactions in collaboration with the ICTR regulatory staff
Recruits, screens, and enrolls research participants. Assists Principal Investigator with informed consent
Coordinates all treatments and tests with associated inpatient and outpatient facilities and staff
Follow-up with patients during each clinic visit to answer questions and assess for toxicities
Ability to travel between study site locations

249

Human Studies Research Coordinator Celebration Health Research Institute Celebration Resume Examples & Samples

BS in health-related field, OR
Bachelors degree in Science or Biology OR
4 years experience coordinating research data and projects in the biomedical field
Specialized knowledge of the current internal and external regulatory needs of clinical trials
Personal qualities and interpersonal communication skills to interact and maintain good relationships with a broad spectrum of healthcare disciplines and the public under all circumstances
Detail oriented and teamwork skills
Motivated, organized, able to perform multiple tasks in a timely manner, and work efficiently under pressure
Ability to manage multiple clinical trials and function independently
Critical thinker and possess an analytical approach to problem solving
Ability to perform diverse administrative duties
Expert knowledge of Microsoft Office applications of Word, Excel, Access, Outlook, and Internet
Ability to adapt own approach according to investigator’s level of expertise to assure all institutional needs are met while learning occurs
Prior research experience (preferred)
Certificate from Clinical Research professional organization, i.e. SOCRA, ACRP (preferred)

250

Assistant Clinical Research Coordinator Resume Examples & Samples

High School graduate with background in science and physiology
Experience working with a research group focused on disparities in the epidemiology or treatment of chronic conditions (i.e., hypertension)
Experience working directly with or research of low-income, safety-net patient populations and their healthcare providers
Excellent verbal and written communication and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team
With guidance from supervisors and PIs ability to abstract data from medical records and transfer them to data collection forms or directly into databases
Experience working with clinical data to improve processes of care (i.e. data from chronic disease registries)

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