Regulatory Assistant – Clinical Trials Office

Role Overview

• Provides support to assure research protocols are in compliance with university, state and federal regulations.
• 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.

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.

Benefits

• Medical, dental and vision coverage, with Ohio State paying a significant portion of the cost.
• Paid time off, including sick and vacation time and 11 holidays.
• State retirement plan or an alternative retirement plan, both with generous employer contributions.