Regulatory Affairs CMC Lead Gene Therapy (Remote)

A leading gene therapy company is seeking an Associate Director for Regulatory Affairs, CMC. This role will manage CMC strategy and coordinate regulatory activities to ensure timely registration of gene therapy products. Candidates should have over 8 years of CMC drug development experience and extensive knowledge of regulatory submissions for gene therapy. The position offers the chance to drive innovative regulatory strategies and ensure compliance with industry standards onsite or in a remote work setting. #J-18808-Ljbffr