Clinical Study Supply Manager H/F - 95

Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions guided by our values Energy, Care and Audacity.

Founded in 2014 and headquartered in Paris, France, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas.

We take a one-team approach to work : our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.

Excelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.About the Job

Join Excelya, whereAudacity, Care, and Energydefine 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)