Excelya

Medical Reviewer for Clinical Data

🇬🇷 Athens, Grecia Híbrido Jornada completa Publicado May 29, 2026
Ubicación Athens, Grecia
Modalidad Híbrido
Contrato Jornada completa
Idioma English
Publicado 29 de mayo de 2026
Última verificación 31 de mayo de 2026
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Medical Reviewer for Clinical Data at Excelya: Athens, Grecia; Híbrido; Jornada completa. JobGrid adds normalized role facts, source context, and a path to the employer application page so candidates can compare the listing before applying.

  • Location and workplace: Athens, Grecia, Híbrido
  • Role classification: Jornada completa
  • Source freshness: checked by JobGrid on 2026-05-31.
  • Application path: candidates continue to the employer application page with non-personal referral tags.

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.