Excelya

Medical Reviewer for Clinical Data

🇧🇪 Brussels, Belgique Hybride Santé et sciences Temps plein Senior Publié Mai 29, 2026
Mode de travail Hybride
Contrat Temps plein
Seniorité Senior
Catégorie Santé et sciences
Langue English
Publié 29 mai 2026
Dernière vérification 31 mai 2026
Contexte JobGrid

Résumé du poste par JobGrid

Medical Reviewer for Clinical Data at Excelya in Brussels, Belgium, is a senior, full-time hybrid role in Healthcare & Science. JobGrid normalizes the role facts from the source posting, keeps the employer content separate, and sends candidates to the original public application page with referral parameters appended.

  • Source posting: 2026-05-29; last checked by JobGrid: 2026-05-31.
  • Workplace: hybrid; location: Brussels, Belgium; employment: full time; seniority: senior.
  • Work language is English; no salary was provided in the payload.
  • Comparable classification on JobGrid: Healthcare & Science.

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 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. 

 

The Study Medical Reviewer is accountable for managing/reviewing the medical consistency of reported clinical data to ensure that medical data in database are accurate, reliable and analyzable. He/Her has the responsibility of his/her studies/projects to provide reliable and consistent data from a medical point of view and to bring medical expertise to all processes from the set-up to the lock of the study.

Main Responsibilities

  • Oversee the medical review process
  • Ensure the reliability of medical data reported in the clinical trials under his/her responsibilities
  • Seriousness review of adverse events
  • Contribute in all processes from the initiation to the completion of clinical trials, thanks to his/her medical expertise
  • Actively participate in Study Team activities as the representative for medical review activities.