Global Regulatory Affairs Lead — Clinical Trial Submissions

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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