Chargement en cours

Clinical Project Manager

ÎLE- E FRANCE, FRANCE
il y a 18 heures
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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Entreprise
Barrington James
Plateforme de publication
WHATJOBS
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