About this opportunity
Centessa Pharmaceuticals lists this Senior Regulatory Project Manager - Global Submissions opportunity in boston, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Centessa Pharmaceuticals in Boston seeks an Associate Director of Regulatory Project Management to lead regulatory projects across development programs. You will own timelines, ensure compliant submissions to health authorities, and partner with Clinical, Nonclinical, CMC, Quality, and Commercial teams to align milestones and resources.
This role requires 8+ years in regulatory affairs, strong planning and communication skills, and proficiency with PM tools.
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.