IQVIA is seeking a Senior Clinical Research Associate (cFSP sponsor-dedicated) in Reading to monitor sites and manage study data per protocol and GCP. You will coordinate monitoring visits, support recruitment plans, and ensure regulatory compliance across assigned sites.
The role requires at least 2 years of on-site monitoring, strong English communication, and solid organizational skills to oversee data quality, site collaboration, and documentation across trials.
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Slough, Berkshire
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
Reading
IQVIA cFSP (sponsor-dedicated) seeks experienced Clinical Research Associates in the UK.
Reading
Applylocations: Reading, Berkshire, United Kingdom: Manchester, United Kingdom: Livingston, West Lothian, United Kingdom: London, United Kingdomtime…
Reading
Join Us on Our Mission to Drive Healthcare ForwardIQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.Why…
London
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
Reading
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by…
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