You are in charge of planning and coordinating clinical studies in compliance with methodological and ethical standards within a leading laboratory. You participate in the drafting of the study protocols, organize the invitations to tender with service providers and negotiate the budget with the purchasing department.
You draw up the specifications, ensure the administrative follow-up of the studies according to BPC-ICH criteria and participate in the drafting of reports. You play an important role in coordinating and supervising the service providers’ activities and the internal ARC throughout the study.

You have a specialized degree in clinical research (DiuFARC, DiuFIEC or CESAM) and a minimum of 2 to 4 years of experience in a similar position in an international context, which has confirmed your scientific and management skills.