Global Project Manager late phase oncology

Excelya; Paris; Sur place; EUR 45 000 - 70 000; Plein temps

Résumé du poste

A progressive clinical research organization in Paris seeks a Clinical Operations professional to lead cross-functional teams and ensure compliance with Good Clinical Practice (GCP). The ideal candidate has a Master's or Pharmacist degree, excellent communication skills, and thrives in collaborative environments. Join a dynamic team dedicated to impact in clinical research while enjoying a stimulating professional growth environment.

Qualifications

• Proven ability to thrive in collaborative, fast-moving environments.
• Bilingual in French and English.

Responsabilités

• Lead and coordinate execution with internal teams.
• Validate and monitor CRO project plans.
• Ensure compliance with Good Clinical Practice (GCP).
• Facilitate communication between internal teams and CROs.
• Manage cross-functional clinical teams and external providers.
• Supervise study operations from startup to completion.
• Monitor trial budgets and vendor selection.
• Track study progress and ensure high-quality data.
• Support quality assurance and continuous improvement.

Connaissances

Strong organizational abilities

Problem-solving mindset

Excellent communication skills

Formation

Master or Pharmacist degree

Description du poste

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 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 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.

Requirements

• Experience: Proven ability to thrive in collaborative, fast-moving environments (avoid requiring minimum years—talent matters most to us!).
• Skills: Strong organizational abilities, problem-solving mindset, and excellent communication skills.
• Education: Master or Pharmacist degree.
• Languages: French & English mandatory.

About You

At Excelya, taking audacious steps is encouraged, so we're looking for individuals who are ready to grow with us and share our values.

Benefits

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 natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.