Regulatory Compliance Assistant to provide support to assure research protocols are in compliance with university, state and federal regulations across research groups managed by the College of Medicines Center for Clinical Research Management (CCRM); 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 and e-Regulatory; assists with monitoring visits; assists with regulatory issues; creates and maintains regulatory files.

Minimum Education Required

High School diploma or GED. Certification or vocational training may be preferred.

Preferred Education

Bachelor's degree, preferably in biological sciences, health sciences, or life sciences

Required Experience

1 year of relevant experience required.

Preferred Experience

2-4 years of relevant experience preferred. Experience in a clinical research capacity desired; computer skills required with knowledge of database software applications desired.

Requires successful completion of a background check. Selected candidate may be requested to complete a pre-employment physical including a drug screen.

FUNCTION/SUBFUNCTION: Research Administration/Research Compliance

CAREER BAND: Individual Contributor-Technical

CAREER LEVEL: T2

This is a hyrbrid position with the majority of job duties being able to be completed remotely; however, individuals may need to come to the office for specific trainings, group meetings/gatherings, etc.

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