Regulatory Assistant

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

Minimum Education Required

Bachelor's degree in biological sciences, health sciences, life sciences or related field, or equivalent combination of education and experience required.

Qualifications

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.