Clinical Project Manager Oncology women health

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

Résumé du poste

Excelya recherche un leader pour les opérations cliniques, jouant un rôle clé dans la gestion d'essais cliniques. Le candidat idéal a une formation en pharmacie ou sciences de la vie, maîtrise l'anglais et le français, et possède une solide expérience en gestion de projet dans un environnement dynamique. Rejoindre Excelya, c'est faire partie d'une équipe ambitieuse qui valorise l'innovation et le développement personnel tout en contribuant à l'excellence dans la recherche clinique.

Qualifications

• Compétences en gestion de projet dans l'industrie pharmaceutique.
• Capacité à travailler dans des environnements collaboratifs et rapides.
• Maîtrise du français et de l'anglais.

Responsabilités

• Leadership opérationnel d'un essai clinique de Phase 3.
• Coordination et supervision des équipes de terrain.
• Assurer la conformité avec les délais, le budget et les normes de qualité.

Connaissances

Gestion de projet clinique

Communication

Leadership

Organisation

Formation

Diplôme en Pharmacie ou Sciences de la Vie

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

• Operational leadership of a Phase 3 clinical trial.
• Coordination and oversight of field teams: CRAs, Lead CRAs, and process support staff.
• Planning and execution of clinical operations activities.
• Ensure compliance with project timelines, budget, and quality standards.
• Preparation for and participation in regulatory inspections and audits.
• Regular reporting to the study leadership team.
• Close collaboration with cross-functional departments (Data Management, Regulatory Affairs, Pharmacovigilance, etc.).

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 (talent matters most to us—no minimum years required).
• Skills: Experience in clinical project management within the pharmaceutical industry or CRO, preferably on interventional international studies in oncology. 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.