Clinical Research Coordinator : Essential Duties and Responsibilities: To perform this job successfully, and individual must be able to perform each essential duty satisfactorily. Other duties may be assigned. • Assist with the preparation and Submission of Regulatory Documentation to Institutional Review Boards and Sponsor • Maintain accurate and organized regulatory documentation, correspondence, safety reports • Follow-up with research subjects • Attends Investigator meetings and educational meetings as necessary • Assist with the maintenance of Institutional Review Board documentation and meet deadlines for submission, continuing review and safety updates • Act as liaison with research collaborators as necessary to coordinate research efforts • Coordination of recruitment including request for referrals, advertising, chart review and database searches • Schedule patient visits, coordinate testing with other departments • Order supplies/ equipment for assigned studies • Generates source documentation and assure accurate collection of data to fulfill protocol design • Communicates with Billing Department regarding research and insurance billing requirements • Completion of Case Report Forms and/or Electronic data capture and respond to queries in a timely manner • Report to and seek guidance from Lead Clinical Research Associate and Principle Investigator as needed • Performs duties as assigned by Primary Investigator and Department Manager • Has awareness of personal limitations. Reports to and seeks guidance from supervisor and/or investigator as appropriate • Works with others on the research team to ensure smooth operation of research program Requirements Qualifications The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential.
Education: a Bachelor’s degree or equivalent work experience
Company address:3702 Pender Drive, Suite 170, Fairfax, VA 22030