Clinical Trials Coordinator - Unlicensed
About The Position
Participate and coordinate in clinical research studies conducted by supervising physician. Perform a variety of administrative duties to assist in the conduct of research trials. Supervises data manager and interns. Responsible for study initiation, subject recruitment, follow-up, data management, detailed record keeping and regulatory compliance, report writing, and correspondence with investigators, sponsors/CROs, IRBs, and regulatory authorities. Responsible for the new submission of protocols with subsequent amendments. Some participation in protocol writing. Educate research subjects, physicians, nurses, and ancillary staff on available research studies, study treatment/ required activities, and use/ side effects of investigational study drug. Responsible for initial and continuing education for Good Clinical Practice compliance.
Responsibilities
- Participate and coordinate in clinical research studies
- Perform administrative duties to assist in the conduct of research trials
- Supervises data manager and interns
- Study initiation
- Subject recruitment
- Follow-up
- Data management
- Detailed record keeping
- Regulatory compliance
- Report writing
- Correspondence with investigators, sponsors/CROs, IRBs, and regulatory authorities
- New submission of protocols with subsequent amendments
- Participation in protocol writing
- Educate research subjects, physicians, nurses, and ancillary staff on available research studies, study treatment/ required activities, and use/ side effects of investigational study drug
- Responsible for initial and continuing education for Good Clinical Practice compliance
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What This Job Offers
Job Type
Full-time
Education Level
No Education Listed
Number of Employees
1,001-5,000 employees
