Regulatory Compliance Assistant

Role Overview

• Provide support to assure research protocols are in compliance with university, state and federal regulations.
• Assist with regulatory functions in support of clinical research activity.
• Assist in preparation of protocol submissions to Institutional Review Boards (IRBs) and provide 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 and e-Regulatory.
• Assist with monitoring visits and regulatory issues.
• Create and maintain regulatory files.

Requirements

• High School diploma or GED.
• Certification or vocational training may be preferred.
• 1 year of relevant experience required.
• 2-4 years of relevant experience preferred.
• 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.