Regulatory Program Manager

Highly Competitive
  1. Contract
  2. Project Manager
  3. France
Paris, France
Posting date: 23 Mar 2026
69002

Looking to oversee Regulatory Programs that could revolutionize the future of medicine and drive breakthroughs in patient care?

Proclinical is seeking an experienced candidate who is capable of leading Lifecycle Management projects for a portfolio of pharmaceutical products. This position will involve cross-functional coordination across CMC, regulatory, industrialization and supply.

Role: Project Manager - Lifecycle Management (pharma)
Duration: Approximately 6 months
Location: Île-de-France (hybrid work possible)

Responsibilities:

  • Leading product lifecycle management projects
  • Coordinating CMC, Regulatory, Supply, and Industrialization functions
  • Monitoring project milestones and cross-functional dependencies
  • Facilitating core team meetings, steering committee meetings and progress reporting

Desired Profile:

  • Project management experience in the pharmaceutical industry
  • Strong understanding of CMC activities and interactions with regulatory and industrial teams
  • Experience with variation/lifecycle management projects is a plus
  • Ability to coordinate cross-functional teams

If you are having difficulty in applying or if you have any questions, please contact Peter Duvall at p.duvall@proclinical.com.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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