Irvine On-Site Clinical Studies Lead FDA Submissions
Job in
Irvine, Orange County, California, 92713, USA
Listed on 2026-03-01
Listing for:
Willow Laboratories
Full Time
position Listed on 2026-03-01
Job specializations:
-
Healthcare
Job Description & How to Apply Below
A medical device company located in Irvine, CA is looking for a Clinical Studies Coordinator to oversee the planning and execution of clinical studies to support FDA submissions. The ideal candidate will have 7-10 years of related experience, excellent communication skills, and the ability to manage multiple concurrent studies.
This role offers an opportunity to work hands-on in both office and laboratory environments, ensuring compliance with GCP and supporting innovative product development.
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