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.