Alternance 12 Mois – Affaires Réglementaires Globales Cmc
Sanofi
Marcy, France
Cmc regulatory dossiers
Clinical trial applications
Investigational new drug applications
As an intern in our Global CMC Regulatory Affairs team, you will participate in various regulatory missions within the R&D department
Job Summary
As an intern in our Global CMC Regulatory Affairs team, you will participate in various regulatory missions within the R&D department.
You will contribute to the preparation of CMC dossiers for Clinical Trial Applications in Europe and internationally, Investigational New Drugs in the United States, and common technical documents.
Sanofi offers an attractive remuneration and access to a wide range of benefits, including profit-sharing, employee share ownership plans, and CSE social activities.
Matching Summary
As an intern in our Global CMC Regulatory Affairs team, you will participate in various regulatory missions within the R&D department.
Skills & Requirements
Must-have
CMC regulatory dossiers
Clinical Trial Applications
Investigational New Drug applications
technical documentation preparation
regulatory strategy definition
Nice-to-have
curiosity and communication skills
analytical and synthesis abilities
collaborative team environment
continuous learning and innovation
Key Requirements
Bac+5 in Pharmacy or Engineering
Intermediate English proficiency
Knowledge of regulatory affairs, CTD, CMC, project management