Clinical Trial Manager

il y a 4 semaines

Lille, Nord, France Pharma Recrutement Temps plein

Permanent (‘CDI’) – Lille, France – Hybrid


ABOUT OUR CLIENT

Our client is the French R&D division of a Swiss clinical-stage pharmaceutical company dedicated to identifying, developing, and commercializing novel antibacterial products for serious, life-threatening infections caused by multi-drug resistant (MDR) bacteria.

The company is currently advancing a Phase 2 program in collaboration with esteemed partners such as the University of Lille and GlaxoSmithKline (GSK).


THE OPPORTUNITY

As part of a small, dynamic team based in Lille, France, the Clinical Trial Manager will play a pivotal role by managing clinical trials from initiation to completion.

Reporting to the Chief Development Officer, and working closely with internal teams and external partners, you will:

  • Oversee and manage all aspects of clinical trials, ensuring timelines, quality, and budget targets are met.
  • Develop and review study protocols, ICFs, and clinical study reports.
  • Supervise CRO activities, including site monitoring and study supply forecasting.
  • Ensure compliance with GCP, internal SOPs, and regulatory requirements.
  • Manage regulatory submissions and maintain the TMF.
  • Select, manage, and evaluate external service providers.
  • Coordinate pre-audit activities and CAPA resolutions.



YOUR PROFILE

  • Master’s degree in Life Sciences or Healthcare.
  • Minimum 4 years’ experience in clinical development and trial management.
  • Strong project management skills.
  • You have the autonomy, flexibility, and adaptability required to thrive in a dynamic biotech environment.
  • You are a real team player with a friendly, positive attitude.
  • You are comfortable taking on tasks beyond the initial scope and contributing to cross-functional projects.
  • Fluent in English.
  • French would be an advantage. Other languages would be a plus.
  • Experience with antibiotic therapies would be a plus.
  • Previous CRA/monitoring experience is a plus.



BENEFITS

  • Attractive remuneration package.
  • Opportunity to work in a cutting-edge biotech environment.
  • Premises located within the Institut Pasteur, in the centre of Lille, close to all transport links.
  • Remote work up to 2 days a week.
  • Alternatively, 1 week remote work per month would be considered.
  • 10 additional paid leave days (‘jours de RTT’) on top of the statutory 25 days of annual leave.
  • ‘Statut cadre’ Executive-level employment status with associated benefits.
  • Occasional travel (4-5 times/year).

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