Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; presents this information at regular research staff meetings.
Communication with patients and scheduling of patients for research visits and procedure and thoroughly documenting patient medical history, specimen collection data, adverse events, concomitant medication use, and protocol compliance.
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.
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.
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 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.).
Assist with the database development, new education courses and programs. Work with course coordinators and faculty to assure that curricula content and assignments are created and assigned before course implementation. Coordinate individual lectures with instructors. Facilitate the transfer of course content to web-based versions for ease of use by trainees.