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Salary
≈ $56k – $81k per year (Estimated)
Location
In office (Paris)
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 19, 2026. First seen by Alion on Oct 16, 2026.

Overview
Company
Impact
Profile match
Excelya is a European contract research organisation that supports pharmaceutical, biotechnology and medical device companies in clinical development. It offers full-service clinical trial management, functional service provision and staff resourcing in clinical operations, regulatory affairs, quality assurance and biometrics, with teams in France, Belgium, Germany, Greece and other countries. The company is headquartered in Paris, France.

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.

Requirements

  • 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

Benefits

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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