Clinical Project Manager
Company: Barrington James Agency
- Location: Île-de-France, France
- Seniority: Senior
- Employment type: Full-time
- Posted: Yesterday
- Offer language: English
Job description
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.
- Willingness to travel when required.
