Regulatory Assistant - Clinical Trials Office

The Ohio State University
Remote

About The Position

The Regulatory Assistant will provide support to ensure research protocols are in compliance with university, state, and federal regulations across research groups managed by the Clinical Trials Office (CTO). This role is crucial for maintaining the integrity and compliance of clinical research activities.

Requirements

  • Bachelor's degree, preferably in biological sciences, health sciences, or life sciences or equivalent combination of education and experience required.
  • Computer skills required with knowledge of database software applications desired.

Nice To Haves

  • Experience in a clinical research capacity desired.
  • Knowledge of database software applications desired.

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.

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.
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