Clinical Trials Project Manager

il y a 16 heures


Bordeaux, Nouvelle-Aquitaine, France Pharmiweb Temps plein

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. We accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.

About Medpace

We leverage local regulatory and therapeutic expertise across all major areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. Our mission is to make a difference in the lives of people living with illness and disease.

Finding Success at Medpace

  • Awarded by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024
  • Recognized with CRO Leadership Awards from Life Science Leader magazine for expertise, quality, capabilities, reliability, and compatibility

Our Culture

At Medpace, we value People, Purpose, and Passion. We offer a flexible work environment, competitive compensation and benefits package, and structured career paths with opportunities for professional growth.

What We Offer

  • Competitive salary: $80,000 - $110,000 per year
  • Flexible work environment
  • Competitive compensation and benefits package
  • Structured career paths with opportunities for professional growth
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives

About the Role

This position will join our France, Lyon Clinical Trial Management team as an Associate Clinical Trial Manager. The successful candidate will be responsible for communicating and collaborating on global study activities, working closely with project coordinators and clinical trial managers.

Responsibilities

  • Communicate and collaborate on global study activities
  • Compile and maintain project-specific status reports within the clinical trial management system
  • Interact with internal project teams, sponsors, study sites, and third-party vendors
  • Provide oversight and quality control of internal regulatory filing systems
  • Create and maintain project timelines
  • Ccoordinate project meetings and produce quality minutes

Qualifications

  • PhD in Life Sciences
  • Fluency in English with solid presentation skills
  • Ability to work in a fast-paced dynamic industry within an international team
  • Prior experience within the CRO or pharmaceutical industry not required but advantageous

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