Clinical Trial Project Lead — France (Multicentre)

Barrington James; Île-de-France; On-site; EUR 70,000 - 110,000; Full time

Job summary

Barrington James in France is seeking an experienced Clinical Project Manager to lead the planning, coordination and delivery of multicentre clinical studies from initiation to close-out. You will act as the primary point of contact for sponsors, investigators and external partners, ensuring timelines, budgets and resources are aligned.

The role requires a Bachelor's degree in a scientific or healthcare field, at least 5 years in clinical research, and strong knowledge of ICH-GCP and European

Qualifications

• Bachelor’s degree in a relevant scientific or healthcare field.
• Minimum 5 years’ experience in clinical research.
• Experience managing clinical studies or projects within a CRO, sponsor or clinical research environment.
• Strong understanding of clinical trial regulations, ICH-GCP and 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; French language skills considered advantageous.

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 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 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.

Skills

Project management

Stakeholder management

Budgeting

Timeline planning

Communication

Cross-country coordination

English fluency

Education

Bachelor's degree in a relevant scientific or healthcare discipline

Job description

Barrington James in France is seeking an experienced Clinical Project Manager to lead the planning, coordination and delivery of multicentre clinical studies from initiation to close-out. You will act as the primary point of contact for sponsors, investigators and external partners, ensuring timelines, budgets and resources are aligned.

The role requires a Bachelor's degree in a scientific or healthcare field, at least 5 years in clinical research, and strong knowledge of ICH-GCP and European