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 Required Qualifications

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.

Base Pay: $20.00 / Hour

This position is primarily remote with an occasional need to work onsite in Columbus. Ohio residency is required.

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About The Ohio State University

The Ohio State University is a dynamic community of diverse resources, where opportunity thrives and where individuals transform themselves and the world. Founded in 1870, Ohio State is a world-class public research university and the leading comprehensive teaching and research institution in the state of Ohio. With more than 63,000 students (including 57,000 in Columbus), the Wexner Medical Center, 14 colleges, 80 centers and 175 majors, the university offers its students tremendous breadth and depth of opportunity in the liberal arts, the sciences and the professions.

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