COME AND JOIN US!
We are looking for a Clinical Research Associate
The main tasks that you will be entrusted with are the following:
- To carry out monitoring visits, from initiation to closure, for all types of phase 1 to 3 studies as well as for clinical investigations of medical devices.
- Prepare submission dossiers for ethics committees and regulatory authorities
- Manage the entire Trial Master File
Teleworking is possible.
You have a scientific background and a first experience with GCP. You will be able to work independently, be rigorous and reactive and have good interpersonal skills. You are fluent in English in a professional context.