About this opportunity
BeiGene, Ltd. lists this Global Regulatory PM Director - Submissions & Strategy opportunity in northern, Kentucky. Review the employer’s description below for duties, qualifications and application requirements.
Job description
BeOne Medicines Ltd. seeks an Associate Director, Global Regulatory Project Management to lead regulatory strategies and submissions across the global development lifecycle. You will partner with GRL/RRL, drive cross‑regional projects, and ensure timely regulatory deliverables.
The role requires 8+ years in regulatory PM, with experience across IND/CTA and NDA/BLA/MAA, plus strong leadership and stakeholder skills in a global context. Travel may be required as projects demand.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.