Global RWE project Manager Rare Disease – France

Excelya>All job opportunites>Full-time, Permanent Contract>Global RWE project Manager Rare Disease – France

Job description

Why Join Us?

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

Here’s what makes us unique

We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s leading mid-size CRO with the best employee experience. Our one-stop provider service model—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient’s journey.

Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Responsibilities

  • Lead the study Cross Functional Team (CFT) during the preparation phase, overseeing study design and kick-off.

  • Initiate and maintain high-level feasibility assessment, adjusting with protocol changes.

  • Develop and manage project budgets, including clinical supply forecasting.

  • Drive the Service Provider (SP) selection process: draft RFPs, lead bid defenses, and manage contracting in collaboration with procurement and legal teams.

  • Finalize the Integrated Oversight Plan (IOP) before study initiation, defining KPIs, QTLs, and performance metrics with stakeholders.

  • Coordinate study conduct, ensuring SP and internal team performance meets timelines and budget expectations.

  • Continuously monitor delivery of KPIs/QTLs as outlined in the IOP.

  • Review site visit reports and ensure timely resolution of issues raised by monitors, cross-functional teams, or CROs.

About You

At Excelya, taking audacious steps is encouraged, so we’re looking for individuals who are ready to grow with us and share our values.

  • Experience: Proven ability to thrive in collaborative, fast-moving environments (avoid requiring minimum years—talent matters most to us!)
  • Skills: Experience in pharmaceutical drug development with a strong background in project management of international studies, Demonstrated project leadership skills and the ability to drive cross-functional collaboration.
  • Education: Master or Pharmacist’s degree 
  • Languages: French & English mandatory

 

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