Regulatory 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).Responsibilities: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 statusAssists in preparation of other required regulatory documentsDistributes approved documentsRelays information to clinical research staffAssists with data entry including collecting, entering and maintaining data and documents in the OnCore electronic databaseAssists with monit