Global Clinical project Manager Rare disease – France

TN France; France; Sur place; EUR 50 000 - 90 000; Plein temps

Résumé du poste

Join a dynamic and ambitious team in Clinical Operations at a forward-thinking company focused on redefining excellence in healthcare. As a Global Clinical Project Manager, you will lead innovative clinical research projects, ensuring compliance with regulations and driving collaboration among diverse teams. This role offers a stimulating environment that fosters personal and intellectual growth, allowing you to make a significant impact on patient journeys. If you're passionate about advancing clinical research and thrive in a collaborative setting, this opportunity is perfect for you.

Qualifications

• Experience in leading clinical projects and managing cross-functional teams.
• Strong understanding of GCP and regulatory compliance.

Responsabilités

• Lead and coordinate execution with internal teams and CROs.
• Ensure compliance with GCP and local regulations.
• Monitor and control trial budgets and study progress.

Connaissances

Clinical Research

Project Management

Good Clinical Practice (GCP)

Risk Mitigation Strategies

Team Leadership

Formation

Bachelor's Degree in Life Sciences

Master's Degree in Clinical Research

Description du poste

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Global Clinical Project Manager Rare Disease – France, France

Client: Excelya

Location:

Job Category: Other

EU work permit required: Yes

Job Reference: cedbee0e26e8

Job Views: 2

Posted: 27.04.2025

Expiry Date: 11.06.2025

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 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 offers 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 clinical research, while enjoying a stimulating environment that encourages personal and intellectual growth.

Main Responsibilities:

• Lead and coordinate execution with internal teams, including Medical Directors and Clinical Development leaders.
• Validate and monitor CRO project plans, ensuring alignment with study objectives and risk mitigation strategies.
• Ensure compliance with Good Clinical Practice (GCP), local regulations, and internal guidelines.
• Facilitate communication and collaboration between internal teams, CROs, and investigators.
• Manage and guide cross-functional clinical teams and external service providers.
• Supervise study operations, from startup to completion, including feasibility assessments, site selection, and regulatory processes.
• Monitor and control trial budgets, vendor selection, and contract negotiations.
• Track and report study progress, addressing deviations and ensuring high-quality data.
• Support quality assurance, audits, and continuous improvement initiatives across clinical projects.