From the 19 March 2020
You come from a scientific (PhD) or medical (Doctor, Pharmacist) training, you master the regulations related to clinical studies and are bilingual in English.
You have proven experience in medical writing and have particular knowledge of CERs or BERs.
In a laboratory specialized in medical devices, located in Ile-de-France, you are attached to the research department.
Autonomous, you are responsible for developing development plans as well as writing pre-clinical and clinical studies, drugs, regulatory files, periodic safety reports and answers to questions from health authorities.
In connection with your hierarchy, you also monitor service provider studies and coordinate the “medication” activities that fall to you.
The different steps to integrate the tribe
- First telephone exchange with a person from the HR team
- Technical interview with a Business Engineer
- Physical meeting in our offices and constitution of the skills file
- Last exchange with one of our managers