Clinical Research Coordinator 2 - Cancer Institute
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About The Position
The Clinical Research Coordinator II of Cancer Clinical Research Office (CCRO) is an integral member of the research team. The Clinical Research Coordinator works independently to support the Principal Investigator by providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. 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. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Ensures the data quality and integrity for each clinical trial and communication with the Principal investigator, Manager and oversight bodies. While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
