The Clinical Research Coordinator III in addition to the duties and responsibilities of a CRC II, the CRC III has added responsibilities which include assisting with the training of new staff, providing assistance with TACL protocol development, developing policies and procedures, and supporting regulatory submissions (e.g. IND applications and maintenance, MedWatch forms, IRB application and renewal, etc.).
Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
The Clinical Research Coordinator II serves as clinical research project manager on several additional externally-funded research projects in Hematology Oncology. Contributes to design of research projects to meet proposal goals established by the PI and sponsor.