Excelya

Medical Reviewer for Clinical Data

🇬🇷 Athens, Grèce Hybride Temps plein Publié Mai 29, 2026
Mode de travail Hybride
Contrat Temps plein
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 is a hybrid, full-time role in Athens, Greece. JobGrid normalizes the location and employment facts, keeps the source in English, and preserves the original public application path. The listing was posted on 2026-05-29 and last checked on 2026-05-31; no salary is provided in the payload.

  • Role title: Medical Reviewer for Clinical Data at Excelya in Athens, Greece.
  • Workplace and employment: hybrid, full time.
  • Source freshness: posted on 2026-05-29 and last checked on 2026-05-31.
  • Language boundary: the source content is in English; JobGrid keeps the publisher-facing copy tied to structured job facts only.

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.