Global Regulatory Affairs Lead — Clinical Trial Submissions
Job in
Kingston upon Hull, Hull, East Riding of Yorkshire, HU2, England, UK
Listed on 2026-07-06
Listing for:
Simbec-Orion
Full Time
position Listed on 2026-07-06
Job specializations:
-
Healthcare
Healthcare Compliance, Clinical Research, Medical Science Liaison
Job Description & How to Apply Below
Simbec-Orion is looking for a Senior Regulatory Affairs Associate to join their Regulatory Affairs & Technical Writing team in the United Kingdom. This role involves coordinating Global Clinical Trial applications of medical products and ensuring compliance with ICH and Regulatory guidelines.
The ideal candidate will have extensive experience in clinical trial submissions, a Bachelor's degree in a Science or Medical field, and strong analytical skills. Fluency in English is required, and knowledge of another European language is desirable.
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