Global Regulatory Submissions Program Lead
Listed on 2026-10-30
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Pharmaceutical
Healthcare Compliance
Centessa Pharmaceuticals is seeking a Regulatory Program Lead to develop and maintain integrated project plans for global regulatory submissions, ensuring adherence to scope, timelines, budgets, and quality standards.
You will act as the primary regulatory timeline liaison across Clinical, Nonclinical, CMC, Quality, and Commercial functions, coordinating cross-functional teams and mitigating risks while preparing for agency meetings.
Step into the Global Regulatory Submissions Program Lead role at Centessa Pharmaceuticals in United States and grow with us.
We would love to welcome a new Global Regulatory Submissions Program Lead to our team in United States.
For the Global Regulatory Submissions Program Lead position at Centessa Pharmaceuticals, we are reviewing applications now.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
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