Clinical Research Regulatory Specialist
Listed on 2026-10-11
-
Healthcare
Healthcare Compliance, Clinical Research, Medical Science
University of California, Irvine seeks a Regulatory Affairs professional to independently manage the regulatory lifecycle of clinical studies, including activation, submissions, amendments, and closeout. You will prepare and oversee all regulatory documents and collaborate with investigators, sponsors, and regulators to maintain compliance.
Ideal candidates have 3–5 years regulatory experience, knowledge of FDA/GCP/IRB processes, and proficiency with OnCore or Complion in a healthcare research
This posting is for the Contract Clinical Research Regulatory Specialist role at UC Irvine, based in Orange, CA, United States.
As a Contract Clinical Research Regulatory Specialist, you will play an important part at UC Irvine in Orange, CA, United States.
We invite applications for the Contract Clinical Research Regulatory Specialist position located in Orange, CA, United States.
The following role is for a Contract Clinical Research Regulatory Specialist with UC Irvine.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).