CMC Regulatory Lead – Pediatric Drug Development

Vor 3 Tagen


Zug, Schweiz Actalent Vollzeit

A biotech consulting firm is seeking a Senior CMC Regulatory Affairs Project Consultant to manage regulatory strategy and submissions for pediatric programs. The ideal candidate has over 10 years of experience in drug development and extensive knowledge in authoring CMC sections of regulatory documents. This position offers a 50% contract with the opportunity to work in a fast-paced environment focused on improving disease management and patient care.
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