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 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.
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 Lab Scientist Coordinator performs chemical, microscopic, and/or bacteriologic tests and verifies results for use in the diagnosis and/or treatment of disease. This position also coordinates the technical operations of the laboratory sections for which responsible while also demonstrating competency in patient testing for neonate, pediatric, adult, and geriatric patients.
This position is responsible for completing analyses and developing manuscripts for cohort studies at the San Francisco Coordinating Center (SFCC), focused on clinical and translational research about aging.