Regulatory Assistant - CCC | Clinical Trials Office

Position Summary

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 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

Job Requirements

Bachelor's degree, preferably in biological sciences, health sciences, or life sciences or equivalent combination of education and experience required; experience in a clinical research capacity desired; computer skills required with knowledge of database software applications desired.

As one of only 50 designated comprehensive cancer centers in the nation, The Ohio State University Comprehensive Cancer Center Arthur G. James Cancer Hospital and Richard J. Solove Research Institute is dedicated to the creation of knowledge in laboratory, clinical and population-based cancer research. We apply those discoveries to develop more effective approaches to cancer prevention, diagnosis, and therapies providing tomorrows standard of care today. A Cancer-Free World Begins Here.