Clinical Project Manager

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

Résumé du poste

Excelya recherche un professionnel en gestion de projets cliniques pour son équipe dynamique en opérations cliniques. Ce poste implique la coordination d'équipes et la gestion de budgets pour des essais cliniques internationaux. Si vous êtes passionné par la science et souhaitez évoluer dans un environnement collaboratif, rejoignez-nous pour redéfinir l'excellence dans le secteur de la santé.

Qualifications

• Capacité éprouvée à prospérer dans des environnements collaboratifs et dynamiques.
• Expérience en gestion de projets cliniques dans l'industrie pharmaceutique ou CRO.
• Fluente en Français et Anglais.

Responsabilités

• Coordonner l'équipe clinique locale pour des essais oncologiques.
• Gérer le budget et le calendrier des études.
• Assurer le recrutement réussi des patients.

Connaissances

Gestion de projet clinique

Communication

Leadership

Organisation

Formation

Diplôme en Pharmacie, Sciences de la Vie ou équivalent

Description du poste

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.

Main 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.

Requirements

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.

• Experience: Proven ability to thrive in collaborative, fast-moving environments (we value talent over minimum years of experience).
• 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.

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.