Clinical Research Regulatory Lead
Listed on 2026-10-11
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Research/Development
Clinical Research, Medical Science, Regulatory Compliance Specialist
The University of California, Irvine seeks a Regulatory Affairs Specialist to independently manage the regulatory lifecycle of clinical research studies, including study activation, IRB submissions, continuing reviews, amendments, and closeout.
You will prepare and oversee all regulatory documents to ensure compliance with FDA, GCP, and sponsor requirements, collaborating with investigators, sponsors, and regulatory agencies.
The Contract Clinical Research Regulatory Lead role at UC Irvine is now open for applications in Fullerton, CA, United States.
This is an excellent opportunity to take on the Contract Clinical Research Regulatory Lead role at UC Irvine.
As a Contract Clinical Research Regulatory Lead, you will play an important part at UC Irvine in Fullerton, CA, United States.
We invite applications for the Contract Clinical Research Regulatory Lead position located in Fullerton, CA, United States.
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