The Per Diem Clinical Research Coordinator-OB/GYN performs the regular duties of a full- or part-time Clinical Research Coordinator on an as-needed basis. Due to the limited number of hours, this position does not apply for Exempt status as is normal in this group. The coordinator assists with clinical research studies by obtaining informed consent, collecting and organizing study information, and potentially performing phlebotomy. The role also supports preparation of grant applications and documents for the Institutional Review Board (IRB) and Grants and Contracts Office (GCO).
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Education Level
No Education Listed