Global Clinical Project Manager
Excelya Paris, Ile-de-France, France
Pharmaceutical Manufacturing · 501-1,000 employees
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About the role
Lead and coordinate the operational conduct of international clinical studies in pediatric oncology while overseeing timelines, budgets, and quality objectives. Manage relationships with stakeholders, ensure regulatory compliance, and facilitate cross-functional team collaboration.
What they look for
Requirements
Requires a degree in Life Sciences, Pharmacy, Medicine, or a related field along with significant experience in clinical project management. Candidates must possess strong knowledge of international clinical trials, ICH-GCP guidelines, and experience managing CROs and vendors.
Full description
Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.
We are looking for a Senior Clinical Project Manager to support the operational management of an international clinical trial in pediatric oncology. This role offers the opportunity to work in a highly collaborative environment and contribute to innovative research programs with global impact.
Key Responsibilities
- Lead and coordinate the operational conduct of international clinical studies.
- Oversee study timelines, milestones, budget, and quality objectives.
- Manage relationships with investigational sites, CROs, vendors, and study stakeholders.
- Ensure compliance with ICH-GCP, regulatory requirements, and study procedures.
- Monitor study progress, patient recruitment, and site performance.
- Identify risks and implement mitigation plans to ensure successful study delivery.
- Coordinate cross-functional teams and facilitate project governance meetings.
- Contribute to study reporting, inspection readiness, and continuous process improvement.
- Degree in Life Sciences, Pharmacy, Medicine, or related field.
- Significant experience in Clinical Project Management within clinical research.
- Strong knowledge of international clinical trials and ICH-GCP guidelines.
- Experience managing CROs, vendors, budgets, and study timelines.
- Previous exposure to oncology and/or pediatric clinical studies is highly desirable.
- Excellent communication, stakeholder management, and leadership skills.
- Fluent in English
Why join us?
At Excelya, we combine a passion for science with the enthusiasm of teamwork to redefine excellence in healthcare.
Here's what makes us unique:
We are a young and ambitious healthcare company, bringing together 900 Excelyates, driven by the goal of becoming the leading mid-sized CRO in Europe, while offering the best employee experience.
Our "one-stop provider" service model—combining full-service, functional service provider, and consulting—allows you to grow through diverse and stimulating projects. By collaborating with leading experts, you will contribute to the development of scientific, operational, and human knowledge, all in service of improving the patient journey.
Excelling with kindness means evolving in an environment that values your natural talents, encourages boldness, pushes boundaries, and cultivates your potential, so that you can fully contribute to our shared mission.
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