Clinical Research Coordinators in the Division of GYN Oncology support multiple externally funded investigator initiated and cooperative group clinical trials. The CRC will be responsible for patient screening, subject enrollment, scheduling, collecting, storing and shipping biological samples; collecting and filing study documents; and collecting and entering clinical data. Utilizing a variety of electronic systems, the CRC will document study activities with accuracy. The coordinator may assist with Institutional Review Board (IRB) filings and inquiries and with manuscript preparation, grant proposals, and research related presentations. The CRC will oversee 2 or more clinical trials, ensuring that the protocol integrity is maintained, all data and queries are answered in a timely manner, and AEs and SAEs are appropriately reported to the sponsor and IRB per protocol. In addition to the responsibilities mentioned above, The CRC will take an active role in preparation of trial audits and inspections. The CRC will assist with mentoring research assistants.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Job Type
Full-time
Career Level
Entry Level