PV officer – France

Job description

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.

About the Job

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 Safety. 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

  • Review cases entered in the LAM of ARGUS to assess whether the information is sufficient to create a valid pharmacovigilance case.
  • Route complete cases from LAM to the central ARGUS safety database when they meet the required criteria for case creation (e.g., valid ICSR).
  • Document comments in LAM when the submitted case does not fulfill the definition of a reportable pharmacovigilance case.
  • Update and maintain tracking tools (e.g., case review tracker) to ensure clear documentation of review activities and timelines.
  • Collaborate with local affiliate teams or global PV functions as needed for clarification or follow-up on case content.
  • Ensure compliance with global PV regulations, SOPs, and data integrity standards.

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 (avoid requiring minimum years—talent matters most to us!)
  • Skills: Basic understanding of ICSR requirements (4 minimum criteria: identifiable reporter, patient, suspect product, and adverse event), Familiarity with ARGUS Safety Database; experience with LAM is a strong advantage.
  • Education: Degree in Life Sciences, Pharmacy, Nursing, or a related health/science discipline.
  • Languages: Fluency in French & English

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