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 €/month + meal vouchers (10€/day worked) + 100% refunded transport pass (limit 80 €/month)
A permanent contract can be offered at the end of the apprenticeship.
POSTULER