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.).
The Clinical Research Coordinator II is primarily responsible for clinical data mining and database input. The CRC serves as the primary source for faculty and staff for clinical data and program outcomes and performs data queries and analyses.
The Clinical Practice Coordinator (CPC) is an integral part of the Dignity Health Medical Foundation (DHMF) care team. The CPC performs the functions of assessing, planning, implementing and evaluating plans of care for attributed patients.
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.