LYON
- From pre-study to close-out visits (Phase I to IV)
- Performed contracts and financial disclosure
- Project management/coordination of the sites activities(clinical department, pharmacy and peripheral department)
- Management of site material (manufacturing of blood samples kits sending)
- Coordination of adverse events report as well as safety reports
- Expert knowledge of FDA guidelines, GCPs/ICH
- Experience with IVRS, IWRS and RDC
- Therapeutic areas: Oncology, Pneumology, Multiple sclerosis, HIV, sleeping disorder and nutrition studies
Pas de formation renseignée
