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Excelya
Excelya
501 – 1,000 Employees
ConsultingHealthcareLogistics
Excelya is a global Contract Research Organization (CRO) that helps biotech, pharmaceutical, and medical device companies develop and deliver healthcare products. Operating across 28 countries, the company provides full-service, functional service provider (FSP), and resourcing solutions across a broad range of therapeutic areas. Its collaborative, flexible approach supports clients with the expertise and delivery capacity needed to advance life-changing therapies.
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Senior Clinical Project Manager - Hybrid France

Lead local pharmaceutical clinical trial delivery for Excelya, a European contract research organization. Coordinate regulatory compliance, investigational sites, vendors, recruitment, data quality, and collaboration with global study teams.

FRFranceHybridFull-timeSeniorEnglish RequiredFrench RequiredClinical Operations
Google Cloud Platform

Description

  • Manage local clinical trial activities from study start-up through close-out
  • Deliver global study plans locally while meeting timelines and quality expectations
  • Act as the primary contact for investigational sites and regional stakeholders
  • Maintain compliance with local regulations, ICH-GCP, and internal standard operating procedures
  • Coordinate submissions to competent authorities and ethics committees when needed
  • Track regulatory milestones and oversee corrective actions
  • Support site selection, activation, monitoring, and close-out with CRAs and vendors
  • Manage local vendor relationships across logistics, laboratory, and CRO services
  • Monitor recruitment, site performance, and operational metrics
  • Partner with global study teams and medical, regulatory, and clinical operations functions
  • Attend study meetings and report on local progress, issues, and outcomes
  • Assist with risk mitigation and operational problem-solving
  • Oversee data quality, query resolution, and documentation compliance
  • Monitor KPIs, recruitment, timelines, and operational deliverables
  • Support audit and inspection readiness activities

Requirements

  • Background in clinical operations within a pharmaceutical company or CRO
  • Experience working as a Clinical Project Manager, Study Manager, or in a comparable role
  • Prior participation in interventional Phase II–IV trials is preferred
  • Strong knowledge of ICH-GCP, regulatory requirements, and local clinical research practices
  • Experience working with investigators, CROs, and cross-functional teams
  • Well-developed organizational, operational, and communication abilities
  • Able to prioritize and manage multiple responsibilities in a fast-moving setting
  • Fluent written and spoken French and English

Benefits

  • Build expertise through varied and engaging projects
  • Work alongside recognized industry specialists
  • Help advance scientific, operational, and human knowledge
  • Join a workplace that recognizes individual strengths and supports initiative
  • Develop professionally while contributing to a shared mission
  • Be part of an organization focused on employee experience
  • Work with an ambitious healthcare company and a 900-person team

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