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Job description
Summit Therapeutics seeks a Director of Regulatory Program Management to lead high-priority regulatory filings across the portfolio. The role aligns Research, Development, Regulatory Affairs, and Manufacturing to deliver rigorous, timely submissions and clear governance across programs.
The position partners with Regulatory Affairs, Medical Writing, and leadership to translate strategies into executable plans and drive organizational capability in complex regulatory initiatives.
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Worksite address
palo alto, CA, 94306, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.