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.
In this role, you will combine operational PV expertise with project coordination responsibilities to ensure patient safety and regulatory compliance throughout the product lifecycle.
Main Responsibilities:
Experience: Pharmacovigilance experience within a pharmaceutical company, CRO, or regulatory environment, Strong hands-on experience in PV case processing, signal detection and safety data management
Education: Degree in Pharmacovigilance, Life Sciences, Clinical Development, Pharmacy, or related field.
Technical Skills: Experience with PV databases, ideally Argus Safety., Solid knowledge of MedDRA coding and terminology, Good command of Microsoft Office tools (Excel, Word, PowerPoint, Outlook).
Soft Skills: Proactive, autonomous, and highly organized.
Languages: Fluent in French & English, both written and spoken.
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.
Copyright © 2026 Grabjobs Pte.Ltd. All Rights Reserved.