Médecin du travail Liège - Ardennes (Français et Allemand)
Life Sciences
Clinical
Master
Medior (3+)
Brussels-Capital
Permanent
Fulltime, On-site
Support clinical development by coordinating trials, ensuring data integrity, and maintaining compliance to bring safe and effective therapies to patients.
Clinical Project Manager – Lead clinical studies and ensure compliant delivery.
Clinical Research Associate (CRA) – Monitor sites and ensure GCP compliance.
Clinical Research Administrator – Support trial coordination and documentation.
Senior Clinical Research Associate – Manage complex studies and mentor CRAs.