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Clinical Research Associate / Coordinator - Cancer Center Protocol Office
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- Clinical Research Associate/Coordinator
- The Cancer Center Protocol Office is a centralized research office that supports clinical researchers in all disciplines within the Cancer Center.
- Our office promotes and facilitates clinical research by providing comprehensive services to physicians conducting clinical trials while ensuring compliance with all regulatory requirements.
- The Clinical Research Associate/Clinical Research Coordinator I (CRA/CRC I) works under general supervision to enroll eligible patients to clinical research protocols and manage all aspects of data collection and submission for multiple cancer studies.
- The CRA/CRC I will be the liaison between the clinical team, sponsor, and Institutional Review Board (IRB) to ensure appropriate communication and reporting.
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