Clinical Research Assistant to provide support to assure research protocols are in compliance with university, state and federal regulations across research groups managed by the Clinical Trials Office (CTO); assists with regulatory functions in support of clinical research activity; assists in preparation of protocol submissions to Institutional Review Boards (IRBs) and provides updates on submission status; assists in preparation of other required regulatory documents; distributes approved documents; relays information to clinical research staff; assists with data entry including collecting, entering and maintaining data and documents in the OnCore electronic database; assists with monitoring visits; assists with regulatory issues; creates and maintains regulatory files.
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