Global Clinical Project Manager Early Phase Oncology H/F - 75

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/Medical Affairs. 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 and coordinateexecution with internal teams, including Medical Directors and Clinical Development leaders.
- Validate and monitorCRO project plans, ensuring alignment with study objectives and risk mitigation strategies.
- Ensure compliancewith Good Clinical Practice (GCP), local regulations, and internal guidelines.
- Facilitate communicationand collaboration between internal teams, CROs, and investigators.
- Manage and guidecross-functional clinical teams and external service providers.
- Supervise study operations, from startup to completion, including feasibility assessments, site selection, and regulatory processes.
- Monitor and controltrial budgets, vendor selection, and contract negotiations.
- Track and reportstudy progress, addressing deviations and ensuring high-quality data.
- Support quality assurance, audits, and continuous improvement initiatives across clinical projects.