Global Regulatory Lead, GI & Inflammation Strategy

A global biopharmaceutical company is seeking an Associate Director of Global Regulatory Affairs to lead and manage regulatory strategies for complex projects. This role requires at least 6 years of pharmaceutical industry experience, including 4 years in regulatory affairs. Key responsibilities include overseeing FDA submissions and ensuring compliance with evolving regulations. The ideal candidate will have a scientific background, strong leadership skills, and the ability to navigate regulatory challenges. The position is based in Boston, MA, and offers competitive compensation and comprehensive benefits.
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