💼 Full-Time Position

Associate Director, Global Regulatory Project Management

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BeOne Medicines
📍 Emeryville, CA, United States
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Location
Emeryville, United States
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Posted
June 23, 2026
Type
Full-Time
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Full-Time Opportunity: This is a permanent, full-time position with a competitive package and real career growth potential.

Job Description

**General Description:** The Associate Director, Global Regulatory Project Management (AD, Global RPM) is a strategic leader responsible for translating and executing regulatory strategies across the global drug development lifecycle. This role blends deep regulatory expertise with advanced project management skills, driving successful NDA/BLA/MAA submissions and ensuring cross-functional integration across regions. The AD, Global RPM proactively anticipates regulatory challenges, influences business decisions, and champions process improvements to secure and maintain market access for products worldwide.

**Essential Functions of the Job:**

**Strategic Global Leadership**

+ Translate, implement, and advise on global regulatory strategies for development programs, ensuring alignment with business objectives and long-term vision across all major regions (US, EU, China, APAC, LATAM, etc.).
+ Act as a key advisor to the GRL/RRL, providing strategic regulatory...