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Hybrid CMC Regulatory Affairs Associate Director

Acadia Pharmaceuticals, San Diego

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An established industry player is seeking an Associate Director for Regulatory CMC to lead global regulatory strategies for small molecule therapeutics. This pivotal role involves coordinating with cross-functional teams to ensure compliance and successful submissions to regulatory authorities. The ideal candidate will have extensive experience in CMC regulatory affairs, particularly in small molecule drug development, and will thrive in a fast-paced environment. This position offers an opportunity to make a significant impact on the life-cycle management of innovative therapies that improve patient outcomes. Join a dynamic team dedicated to advancing neuroscience breakthroughs!
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