Within the Full Development department and the Development operations and clinical development service, you will supervise and coordinate whole clinical projects with the support of the clinical study team and internal and external experts. Your missions:  Coordinate and lead clinical studies : writing and/or reviewing the clinical protocol for its feasibility and appropriateness within the early plan of the project,  Manage and supervise your CRA team.  Select and be the communication point for investigators, clinical administrators and subcontractors (CRO, experts...),  Identify main milestones and establish budget and timelines for the study conduct together with the study team. Establish a detailed planning of clinical project,  Build, follow-up and close out study Budget following internal templates and instructions and according to the initially approved budget,  Ensure clinical data reporting and to coordinate data management process,  Collaborate with other department members to promote harmonization of all processes and procedures.