Clinical Research Coordinator (M/F)

RESPONSIBILITIES: Their mission will notably include: Preparing and implementing studies Leading and conducting trials Enrolling and monitoring participants Managing data and quality assurance Closing and promoting projects

PROFILE SOUGHT:

• Scientific or health background, supplemented by CRC training (DIU FARC-TEC, DU ARC, ...)
• At least 4 years of experience in clinical research and project coordination, ideally in a hospital investigator center
• Knowledge of Good Clinical Practice and the research regulatory environment (Loi Jardé, RGPD /MR-001; up-to-date GCP certification)
• Strong ability to organize, prioritize, and manage multiple projects simultaneously
• Autonomy, ability to take initiative, and aptitude to identify difficulties and propose solutions
• Ease in coordinating multiple stakeholders, both internal and external
• Good writing skills and proficiency in IT tools and clinical data management
• Experience in healthcare establishments in the fields of rehabilitation, neurology, or disability, supplemented by experience in medical device studies, will be particularly appreciated
• Professional English