Director, Regulatory Affairs CMC

As the Director of Regulatory Affairs CMC at Acadia Pharmaceuticals, you will lead the development and execution of global regulatory strategies for small molecule therapies from development through commercialization. Your role will involve managing CMC regulatory activities, preparing submissions for regulatory authorities, and providing guidance on compliance and regulatory risks while collaborating with cross-functional teams.

• Competitive base salary
• Discretionary bonus and equity awards
• Medical, dental, and vision insurance
• Employer-paid life, disability, business travel and EAP coverage
• 401(k) Plan with a fully vested company match 1:1 up to 5%
• Employee Stock Purchase Plan with a 2-year purchase price lock-in

• Hybrid model requires working in the office three days per week on average
• Role involves significant responsibility and leadership in regulatory affairs
• No specific mention of the company's technology stack or tools used