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Clinical Project Manager H/F - 75

Description du poste

  • Excelya
  • Paris - 75

  • CDI

  • Publié le 3 Février 2026

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

- Coordinate the local clinical team involved in national and international oncology trials.
- Participate in the development of study documents (protocols, ICFs, CRFs, etc.).
- Manage the study budget and timeline to ensure efficient execution.
- Oversee site and vendor selection, activation, and performance throughout the study.
- Ensure successful patient recruitment through coordinated clinical activities.
- Deliver study results with high quality, on time and within budget.
- Manage regulatory submissions and administrative follow-up in compliance with ICH-GCP and local regulations.
- Lead feasibility assessments and investigator selection.
- Provide transversal management and operational oversight of CRAs.

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