Clinical Study Supply Manager – France

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

• Manage the end-to-end clinical supply operations for assigned studies

• Ensure timely delivery of clinical supplies within budget, in compliance with GxP, SOPs, and internal standards

• Execute and monitor clinical supply activities throughout the study lifecycle

• Define and implement the optimal supply strategy tailored to each study’s framework

• Communicate effectively with the study team to align on supply timelines and needs

• Supervise the clinical supply production plan and ensure on-time execution

• Review and adjust supply strategies to optimize the supply chain and mitigate potential risks

• Act as the main point of contact for the Global Study Manager regarding supply-related topics

• Provide expertise and leadership on all clinical supply aspects of the study

• Contribute to the review of study documentation (e.g., Protocol, Monitoring Plan, Pharmacy Manual, CRA presentations)