Senior regulatory affairs specialist

Excelya>Permanent Contract>Senior regulatory affairs specialist

Description de l'emploi


- 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



- 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



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