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Associate Manager, CMC Regulatory Submissions & Compliance

Regeneron Pharmaceuticals, Crosby, Mississippi, United States, 39633

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A leading biopharmaceutical company is seeking an Associate Manager for CMC Regulatory Submissions Compliance. This role involves coordinating Clinical Trial Application pre-submission reviews and ensuring adherence to regulatory requirements. You will engage cross-functionally to manage documentation and resolve issues effectively. The ideal candidate will have a BS/BA in Chemistry or Biology, at least 5 years of relevant experience, strong communication skills, and a commitment to regulatory compliance. Benefits include comprehensive health programs and a supportive work culture. #J-18808-Ljbffr