About the Job
oin 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 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 :
Experience: Proven experience in pharmacoepidemiology and/or real-world evidence generation within the pharmaceutical, biotech, or CRO environment.
Skills: Strong methodological expertise in study design, data analysis, and interpretation of real-world data, solid understanding of regulatory requirements and best practices for RWE/PE studies. Experience conducting feasibility assessments, bibliographic research, and data source evaluations.
Education: Advanced degree in Epidemiology, Biostatistics, Public Health, or related Life Sciences field (PhD or Master's with relevant experience preferred).
Languages: Fluent in French and in 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.