8 roles found
Reading
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study…
Reading
In this role you drive site monitoring across interventional studies, ensuring GCP/ICH compliance and high-quality data.
Reading
IQVIA is seeking a Senior Clinical Research Associate (cFSP sponsor-dedicated) in Reading to monitor sites and manage study data per protocol and GCP.
Reading
Join Us on Our Mission to Drive Healthcare ForwardIQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.With…
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