Alternance 12 Mois – Affaires Réglementaires Globales Cmc

Sanofi

Marcy l’Etoile, France
Global cmc regulatory affairs
Clinical trial applications
Investigational new drug applications
Participate in the drafting and preparation of CMC dossiers for Clinical Trial Applications and Investigational New Drug applications

Job Summary

  • Participate in the drafting and preparation of CMC dossiers for Clinical Trial Applications and Investigational New Drug applications.
  • Engage in regulatory meetings with various representatives to understand the regulatory strategy for new vaccine projects.
  • Enjoy attractive compensation, social activities, and generous paid time off, including exam preparation days.

Matching Summary

Participate in the drafting and preparation of CMC dossiers for Clinical Trial Applications and Investigational New Drug applications.

Skills & Requirements

Must-have

  • Global CMC Regulatory Affairs
  • Clinical Trial Applications
  • Investigational New Drug applications
  • New vaccine development
  • CMC dossier strategy

Nice-to-have

  • Curiosity and communication skills
  • Analytical and synthesis abilities
  • Collaborative and inclusive environments
  • Continuous learning and digital innovation

Key Requirements

  • Bac+5 in Pharmacy or Engineering
  • Intermediate English proficiency
  • Knowledge of regulatory affairs, CTD, CMC, project management

Work Rights

Not specified

Tailored Resume

Cover Letter