18h ago
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Pharmacovigilance Specialist

FranceFrance·ParisFull-timemid
Laboratory & Life SciencesPharmacovigilance Specialist
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Quick Summary

Requirements Summary

Master's degree in Life Sciences, Pharmacy, or a related field. Experience in Pharmacovigilance and Safety Data Exchange Agreements is a plus. Strong ability to review,

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Laboratory & Life SciencesPharmacovigilance Specialist

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

  • Perform the medical review and assessment of sensitive and complex pharmacovigilance cases based on source documents and medical records.
  • Analyze case documentation to identify, extract and evaluate relevant medical information in accordance with applicable procedures and guidelines.
  • Contribute to the medical and scientific evaluation of safety cases, ensuring the completeness, consistency and accuracy of collected data.
  • Collaborate closely with Pharmacovigilance Operations teams to support case processing activities.
  • Review documentation to identify potential duplicate cases and support their assessment in collaboration with PV teams.
  • Identify potential adverse events and ensure their timely communication for entry into the global pharmacovigilance database.
  • Assess and communicate significant new safety information and follow-up data arising from additional source documentation.
  • Ensure compliance with pharmacovigilance regulations, internal procedures and quality standards.
  • Support continuous improvement initiatives related to medical case review and pharmacovigilance processes.

Requirements

~1 min read
  • Master's degree in Life Sciences, Pharmacy, or a related field.
  • Experience in Pharmacovigilance and Safety Data Exchange Agreements is a plus.
  • Strong ability to review, interpret and analyze medical records and source documentation.
  • Good understanding of pharmacovigilance principles, adverse event reporting requirements and case management processes.
  • Experience handling complex or medically significant safety cases is highly desirable.
  • Strong analytical skills with excellent attention to detail.
  • Ability to assess and synthesize large volumes of medical information.
  • Experience working within global and cross-functional environments.
  • Excellent written and verbal communication skills in English.

What We Offer

~1 min read

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.

Location & Eligibility

Where is the job
Paris, France
On-site at the office

About this job

Posted
Today
Employer
has 44 open jobs on Jobera in 8 countries.

Listing Details

Posted
October 28, 2026
First seen
October 28, 2026
Last seen
October 28, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
67%
Scored at
October 28, 2026

Signal breakdown

freshnesssource trustcontent trustemployer trust

Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions.

Employees
501-1,000
View company profile
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Pharmacovigilance Specialist