Brussels Metropolitan Area
Conduct operational aspects of clinical trials and ensures studies are conducted according to ICH/GCP and all applicable guidelines and according to the POL/SOP/GUI.
•Perform processes supporting the conduct and monitoring of a clinical trial in Belgium. •Verify that the investigator and the investigator’s trial staff are performing the specified trial functions in accordance with the protocol, ICH GCP and any other written agreement between the sponsor and the investigator / institution. •Check the accuracy or completeness of the CRF entries, source data documents, and other trial-related records against each other