MISSIONS
- Prepare the European cores documents package for international diffusion and French submission to the competent authority
- Coordinate operational activities and Quality Check of all deliveries
- Regulatory team training
- Support the manager of the platform
REQUIREMENTS
- Minimum 3 years’ experience in this area
- Master's degree OR PharmD
- A deep understanding of the European regulatory environment for clinical trial
- Project management experience and experience successfully building relationships across a diverse stakeholder team
- Good level of English, Effective oral and written communication skills
- Ability to work on own initiative
