About the role

University of Rochester seeks a Regulatory Research Admin to coordinate and oversee regulatory requirements for clinical research protocols at UR. You will prepare documentation, manage OnCore/Complion entries, and liaise with sponsors and study teams to ensure timely approvals.
Responsibilities include: IRB submissions, maintaining regulatory records, and ensuring compliance with GCP and federal regulations across multiple sites. A Bachelor's degree and 1 year of relevant experience are required.

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JOB OVERVIEW

Experience level

Senior

Location

Chester, NJ

Occupation

Regulatory Affairs Specialists

Industry

Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)

Posted

today

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