Assists CCRM Regulatory Leadership with the daily oversight of the Regulatory team and monitoring of the regulatory research compliance functions across all research sections/disease groups managed by the CCRM.
Participates in interviews for regulatory staff and trains, mentors, and assists with supervising staff.
Serves as the subject matter expert for all regulatory compliance officers within the CCRM by monitoring & ensuring compliance with Institutional Review Boards (IRBs), FDA (Federal Drug Administration), federal, state & industry sponsor regulations.
Answers questions and provides technical support to junior members on the CCRM Regulatory team.

6 years of relevant experience required.
Knowledge of clinical research regulations and compliance issues especially related to the use of human and animal subjects required.
Bachelor's degree or equivalent experience required.
Advanced degree in relevant field may be desirable.

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.

Research Compliance Consultant, CCRM

Key skills