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Reg. Research Specialist
Job Summary: The Regulatory Specialist for the WMC Cancer Center's Cancer Clinical Trials Office (CCTO) is responsible for all aspects involving regulatory requirements for studies and clinical trials. The regulatory specialist will be responsible for submitting protocols and supporting documents to regulatory bodies, including Scientific Review Committee and IRB. The incumbent will report directly to the Medical Director of the CCTO. Responsibilities: * Submit continuations, amendments, generate reports, and maintain research files, including training and delegation logs consistent with the regulatory requirements for research studies/clinical trials, ensuring compliance with all federal and local agencies, inc


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