Medical Reviewer for Clinical Data
Résumé du poste par JobGrid
Medical Reviewer for Clinical Data at Excelya in Montpellier, France, is listed as a hybrid full-time senior role in Healthcare & Science. JobGrid presents the normalized role facts from the structured listing, keeps the employer description separate, and sends candidates to the original public application page with referral parameters appended. The source was posted on 2026-05-29 and last checked on 2026-05-31; no salary was shown in the provided payload.
- Location: Montpellier, France; workplace: hybrid; employment type: full time; seniority: senior.
- Category: Healthcare & Science; title normalized as Medical Reviewer for Clinical Data.
- Source freshness: posted 2026-05-29, last checked 2026-05-31.
- JobGrid keeps the employer description separate and preserves the source boundary on the page; candidates apply via the original public application page with non-personal referral
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.