Provide support for the conduct of international clinical phase 1 to phase 3 in a pharmaceutical product.
Responsibilities include your participation for all tasks bellow:
of the vendors management, supervision and global budget monitoring, and safety data review and validation by dedicated meeting management with Statistic, DM, Safety, Medical writing and Medical, of deviations, set up, vendor selection, specification preparation and budget evaluation, of protocol Amendment and all study document and review for validation, of Clinical Study Report appendices, review, and archiving, Candidate profile in a Master 2 clinical operation understanding of IT tools with GCP and ICH regulations level in English organizational skills person should have excellent written and verbal communication skills, and be well spoken, enthusiastic in order to succeed.
Location :
Montpellier Salary package:
Minimum 1300 â?¬/month meal vouchers (10â?¬/day worked) 100% refunded transport pass (limit 80 â?¬/month) A permanent contract can be offered at the end of the apprenticeship.
