Clinical Data Reviewer — Medical Affairs

Excelya

Brussel Hoofdstad

Sur place

EUR 55 000 - 85 000

Plein temps

14 jours+
Générateur de candidature

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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

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.

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