TMF & Clinical Trials Admin Specialist
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IQVIA LLC is seeking a diligent Clinical Trial Admin to support Trial Master File delivery and collaborate with CRAs and RSU teams in Brussels. You will help update, file and archive essential clinical documentation within SOPs and timelines.
Responsibilities include handling TMF updates, study file reviews for completeness, tracking CRFs and data flow, and acting as a central contact for communications. Strong English, Dutch and French are required.
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Clinical Trials Support Specialist
Il y a 4 jours
Brussel, Brussel-Hoofdstad, Belgique IQVIA Temps plein 25 000 € - 35 000 € ContratIQVIA 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,...
