Remote CMC Project Manager - 12-Month Contract

Pierre Fabre Laboratories; Toulouse; Hybride; EUR 70 000 - 100 000; Temps partiel

Avantages offerts par ce poste

Profit sharing

Health insurance

Public transport support

Résumé du poste

Pierre Fabre Laboratories is seeking a Projet Manager for CMC (CMC-PM) on a 12-month contract at our Toulouse site. You will support the CMC expert team across clinical development from phase 1 to registration, coordinating timelines, meetings, and documentation with partners.

The role offers hybrid work up to 2 days remote per week and a comprehensive benefits package. Ideal candidates hold an MSc or engineering degree in pharmaceutical sciences with at least 5 years' CMC development

Qualifications

• MSc or Engineer in pharmaceutical science and ideally Pharma-related degree.
• Minimum 5 years' experience in planning pharmaceutical development for CMC across phases 1–3, up to registration.
• Strong knowledge of Good Manufacturing Practices (cGMP).
• Experience leading or coordinating with a CDMO/partner in development programs.
• Proven ability to manage programs, budgets, and governance communications.

Responsabilités

• Coordinate CMC subteam activities with respect to timelines.
• Organize internal CMC team meetings and meetings with partners.
• Support CMC subteam planning and budget management.
• Assist CMC Subteam Leader and Governance meeting prep/slide coordination.
• Coordinate preparation and updates of CMC documentation for clinical submissions (IND/IMPD sections, amendments).
• Coordinate and present updates for Module 3 planning ahead of Phase 3/registration.
• Serve as the point of contact for transversal CMC topics within P&O.

Connaissances

CMC coordination

Project management

Budget management

Leadership

Cross-functional collaboration

GxP/cGMP

Formation

MSc or Engineer in pharmaceutical science

Outils

PowerPoint

Description du poste

Pierre Fabre Laboratories is seeking a Projet Manager for CMC (CMC-PM) on a 12-month contract at our Toulouse site. You will support the CMC expert team across clinical development from phase 1 to registration, coordinating timelines, meetings, and documentation with partners.

The role offers hybrid work up to 2 days remote per week and a comprehensive benefits package. Ideal candidates hold an MSc or engineering degree in pharmaceutical sciences with at least 5 years' CMC development