Strategic Regulatory Affairs Lead
Aquestive Therapeutics
Aquestive Therapeutics is seeking a Regulatory Affairs Strategist to lead regulatory strategies supporting approval and lifecycle management of pharmaceutical products. You will liaise with FDA and other agencies to ensure timely submissions for clinical trials, marketing authorizations, and post-approval changes, while guiding cross-functional teams through product development. The ideal candidate has deep knowledge of FDA requirements, IND/NDA processes, and international regulations, with a #J-18808-Ljbffr Aquestive Therapeutics
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