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Associate Director, Regulatory Project Management at Centessa Pharmaceuticals - ApplyBlast

Associate Director, Regulatory Project Management

Centessa Pharmaceuticals

1 month ago

Boston, Massachusetts, United States

Onsite

Full Time

Director

0 applicants

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About this role

The Associate Director, Regulatory Project Management provides project management leadership across Global Regulatory Affairs, supporting assigned development programs and portfolio priorities. Serving as the central hub for regulatory projects, the role is accountable for regulatory project timelines, ensuring effective planning, tracking, execution, and delivery of submissions to health authorities worldwide. The position partners across the Regulatory function to coordinate deliverables, maintain oversight of submission plans, and ensure regulatory documents are complete, accurate, and submitted on schedule.

Responsibilities

Develop and maintain integrated project plans for regulatory submissions and post-approval activities
Coordinate cross-functional deliverables and maintain oversight of submission plans
Identify, assess, and mitigate project risks while creating contingency plans

Skills

Qualifications

Bachelor's degree in a scientific or related field

About Centessa Pharmaceuticals

centessa.com

Company Size

51-200 employees

Founded

2021

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Centessa Pharmaceuticals is a global biopharmaceutical company that uses an asset‑centric, portfolio model to accelerate the development of innovative medicines. With a patient‑centric mission, Centessa advances programs across sleep‑wake, neurological, neurodegenerative and psychiatric disorders — notably pursuing an Orexin Receptor 2 agonist program. The company combines specialized operating subsidiaries and centralized capabilities to move preclinical and clinical‑stage assets efficiently toward regulatory approval and commercialization. Centessa partners with academic and industry collaborators to translate promising science into transformative treatment options for patients.