We are currently supporting a growing organisation in the clinical research sector in the search for an experienced Clinical Project Manager to join its clinical operations team in France.
Key Responsibilities
- Take overall responsibility for the planning, coordination and delivery of clinical studies from initiation through to close-out.
- Act as the primary point of contact for sponsors, investigators, internal stakeholders and external partners.
- Develop and maintain project plans, timelines, budgets and resource allocation.
- Coordinate site feasibility, site selection, site activation and ongoing study management activities.
- Oversee clinical monitoring activities and work closely with CRAs to ensure effective study delivery.
- Coordinate the preparation and review of essential study documentation, including study protocols, informed consent forms and investigator documentation.
- Manage regulatory and ethics committee submissions across relevant countries.
- Monitor patient recruitment, site performance, study milestones and overall project progress.
- Identify potential project risks and implement appropriate mitigation strategies.
- Work closely with Data Management, Regulatory Affairs and other cross-functional departments.
- Ensure the Trial Master File remains complete, accurate and audit-ready.
- Support sponsor meetings, audits, inspections and the preparation of final study reports.
Requirements
- Bachelor's degree or equivalent qualification in a relevant scientific or healthcare discipline.
- Minimum of 5 years' experience within clinical research.
- Previous experience managing clinical studies or projects within a CRO, sponsor or clinical research environment.
- Strong understanding of clinical trial regulations, ICH-GCP and relevant European regulatory requirements.
- Experience coordinating multicentre clinical studies across multiple countries.
- Strong knowledge of clinical project management, study budgets, timelines and resource planning.
- Experience working with investigators, clinical sites, CRAs and external vendors.
- Excellent organisational, communication and stakeholder management skills.
- Fluent English, with French language skills considered advantageous.
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Clinical Project Manager employeur : Barrington James
En tant qu'employeur de choix, notre entreprise offre un environnement de travail dynamique et collaboratif à Dijon, où l'innovation et la qualité sont au cœur de nos activités. Nous valorisons le développement professionnel de nos employés en proposant des formations continues et des opportunités d'évolution de carrière, tout en maintenant une culture d'entreprise axée sur le bien-être et la reconnaissance des contributions individuelles. Rejoindre notre équipe, c'est faire partie d'une organisation qui s'engage à améliorer la vie des patients grâce à des dispositifs médicaux de pointe.
