Clinical Project Manager

Excelya; Paris; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading clinical research organization is seeking a Clinical Operations professional to coordinate local clinical teams for oncology trials. This role requires strong project management and leadership skills, as well as fluency in French & English. The ideal candidate will enjoy a collaborative environment focused on innovation in clinical research, providing a stimulating professional atmosphere for personal growth.

Qualifications

• Proven ability to thrive in collaborative, fast-moving environments.
• Experience in clinical project management within the pharmaceutical industry or CRO.
• Fluency in French & English.

Responsabilités

• Coordinate the local clinical team in national and international oncology trials.
• Participate in the development of study documents.
• Manage the study budget and timeline.
• Oversee site and vendor selection.
• Ensure successful patient recruitment.
• Deliver study results on time and within budget.
• Manage regulatory submissions.
• Lead feasibility assessments and investigator selection.
• Provide operational oversight of CRAs.

Connaissances

Clinical project management

Organizational skills

Communication skills

Leadership skills

Formation

Degree in Pharmacy, Life Sciences, or equivalent

Description du poste

Overview

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. 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.

Responsibilities

• Coordinate the local clinical team involved in national and international oncology trials.
• Participate in the development of study documents (protocols, ICFs, CRFs, etc.).
• Manage the study budget and timeline to ensure efficient execution.
• Oversee site and vendor selection, activation, and performance throughout the study.
• Ensure successful patient recruitment through coordinated clinical activities.
• Deliver study results with high quality, on time and within budget.
• Manage regulatory submissions and administrative follow-up in compliance with ICH-GCP and local regulations.
• Lead feasibility assessments and investigator selection.
• Provide transversal management and operational oversight of CRAs.

Qualifications

About You

• Experience: Proven ability to thrive in collaborative, fast-moving environments (avoid requiring minimum years—talent matters most to us!).
• Skills: Experience in clinical project management within the pharmaceutical industry or CRO, preferably on interventional international studies; strong organizational, communication, and leadership skills.
• Education: Degree in Pharmacy, Life Sciences, or equivalent.
• Languages: Fluency in French & English.

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.