Regulatory Assistant - CCC | Clinical Trials Office

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). Assist with regulatory functions in support of clinical research activity. Assist in preparation of protocol submissions to Institutional Review Boards (IRBs) and provides updates on submission status. Assist in preparation of other required regulatory documents. Distribute approved documents and relay information to clinical research staff. Assist with data entry including collecting, entering and maintaining data and documents in the OnCore electronic database. Assist with monitoring visits and regulatory issues. Create and maintain regulatory files.