Sara Testoni Study Coordinator, Biostatistics & Clinical Trial Unit – IRCCS IRST, Meldola (FC)
Sanofi, Italy
Management of oncological clinical studies from phase I to phase IV for the Uro-Gynecological pathology group: submission to the Ethics Committee, collection and processing of data, interaction with the Sponsor and the CRO (monitoring, quality visit, audit, inspections).