Clinical Project Manager coordinating national and international oncology trials with Excelya. Overseeing study budgets, regulatory submissions, and ensuring high-quality study results.
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
min 5 years of experience in project management and relevant experience as CRA.
Experience in clinical project management within the pharmaceutical industry or CRO, preferably on interventional international studies.
Strong organizational, communication, and leadership skills.
Degree in Pharmacy, Life Sciences, or equivalent.
Fluency in French & English.
Benefits
We combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.
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.
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