IQVIA cFSP (sponsor-dedicated) seeks experienced Clinical Research Associates in the UK. The role involves on-site monitoring and site management to ensure protocol adherence, data quality and regulatory compliance across multiple UK sites.
Responsibilities include initiating and monitoring visits, training site staff, tracking recruitment, and managing trial documentation in TMF/ISF. 1+ year on-site experience preferred; English communication essential.
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Slough, Berkshire
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
Reading
Applylocations: Reading, Berkshire, United Kingdom: Manchester, United Kingdom: Livingston, West Lothian, United Kingdom: London, United Kingdomtime…
London
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
Reading
Join Us on Our Mission to Drive Healthcare ForwardIQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.Why…
Reading
In this role you will monitor and manage clinical sites to ensure studies are conducted in line with the protocol, GCP, ICH guidelines, and sponsor…
Livingston
In this role you will monitor and manage clinical sites to ensure studies are conducted in line with the protocol, GCP, ICH guidelines, and sponsor…
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