Medical Reviewer for Clinical Data

Excelya; Brussel Hoofdstad; Sur place; EUR 55 000 - 85 000; Plein temps

Résumé du poste

Excelya is seeking a Study Medical Reviewer to ensure medical consistency of data in clinical trials within Medical Affairs. You will bring medical expertise from setup to lock of studies, coordinating with the Study Team to drive reliable data.

The role emphasizes cross-functional collaboration, strong data handling skills, and fluency in English and French to support global studies.

Qualifications

• Experience in medical review, oncology, clinical development.
• Ability to work across functions, curiosity, data handling, and prioritization.
• Fluency in French and English.
• Doctors, pharmacists or PhD with med review experience in industry.
• Nice to have knowledge of WHO Drug and MedDRA dictionaries.

Responsabilités

• Oversee the medical review process.
• Ensure the reliability of medical data reported in clinical trials.
• Seriousness review of adverse events.
• Contribute in all processes from initiation to completion of clinical trials.
• Participate in Study Team activities as the medical review representative.

Connaissances

Medical review

Oncology

Clinical development

Medical data handling

Cross-functional collaboration

English

French

Regulatory dictionaries

Formation

Medical degree / Doctor

PhD / Pharmacist

Description du poste

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 the 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

Qualifications

• Experience in medical review, oncology, clinical development, medical expertise
• Ability to work across functions, curiosity, ability to handle large amounts of data, strong organizational skills, ability to prioritize, English
• Previous professional experience: Doctors, pharmacists, PhD with experience in medical review, coming from industry sector
• Fluency in French and English
• Nice to have experience in coding, knowledge of WHO Drug and MedDRA dictionaries

We provide equal opportunities for all and foster a diverse, equitable, and inclusive workplace where humility and boldness work hand in hand.