Medical Reviewer for Clinical Data
Résumé du poste par JobGrid
Senior full-time hybrid Medical Reviewer for Clinical Data at Excelya in Amsterdam, Netherlands, in Healthcare & Science. JobGrid presents the role as structured facts from the source posting, with the employer description kept separate and the original application route preserved. The source was posted on 2026-05-29 and last checked on 2026-05-31; no salary was provided.
- Role facts normalized by JobGrid: Medical Reviewer for Clinical Data, Excelya, Amsterdam, Netherlands, hybrid, full time, Senior, Healthcare & Science.
- Source freshness is included: posted 2026-05-29 and last checked 2026-05-31.
- The content is based on the source payload only; original-language employer wording is not repeated here.
- JobGrid keeps the employer application path intact and sends candidates to the original public application page with non-personal referral parameters.
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.