YOUR RESPONSIBILITIES :

• Collaborate with cross-functional team to develop clinical trial designs and supporting clinical operation team.
• Write protocols, publications and others document as needed, including for regulatory aspects, for all clinical research part.
• Respect clinical trial safety elements for decision making.
• Lead Medical Oversight and Medical Monitoring to interventional clinical trials 
• Evaluate investigator-initiated study protocols and make recommendations to take decision regarding the clinical trial.
• Ensure trainings for internal staff, service providers or investigators

 YOUR PROFILE:

• Master or PhD in the LifeScience with minimum 5 years experience in the same position.
• Strong experience and understanding of clinical research and clinical trial design, data analysis, statistics, and methods.
• Good knowledge of GCP aspects and FDA guidelines.
• Fluent in French and English.
• Open to travel 5 -10% or working time.
• Good leadership and used to work in cross-functional team.