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.
#J-18808-LjbffrSenior Regulatory Project Manager - Global Submissions in boston at Unknown Company
This position is listed as full time and onsite.