Clinical Trials Support Specialist

Il y a 23 heures

Brussel, Brussel-Hoofdstad, Belgique IQVIA Temps plein 25 000 € - 35 000 € Contrat

IQVIA is seeking an administrative professional to support TMF and trial documentation coordination within the Clinical Research framework in Belgium. You will collaborate with CRAs and RSU teams to ensure timely and accurate clinical records and reporting.

The role emphasizes attention to regulatory standards (GCP/ICH) and strong document control skills, with on-site support and potential site visits after training. Proficiency in English, Dutch, and French is required.