Medical Reviewer for Clinical Data
Podsumowanie roli od JobGrid
Medical Reviewer for Clinical Data at Excelya in Freiburg, Germany is a hybrid, full-time Senior role in Healthcare & Science. JobGrid presents the normalized role facts from the structured posting, keeps the employer description separate, and routes candidates to Excelya’s original public application page with referral parameters. The posting was published on 2026-05-29 and last checked on 2026-05-31; no salary was provided in the source payload.
- Role facts normalized by JobGrid: title, company, Freiburg, Germany, hybrid workplace, full-time employment, Senior level, and Healthcare & Science category.
- Source freshness is visible on the page: published 2026-05-29 and last checked 2026-05-31.
- Original-language boundary is preserved: the job content is presented in English from the payload, while the employer description stays separate.
- Applicants are sent to Excelya’s original public application page; JobGrid appends 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.