Onsite Clinical Research Associate - GCP/ICH Expert
IQVIA UK's cFSP (sponsor-dedicated) team is growing, seeking experienced Clinical Research Associates to monitor interventional studies in the UK. You will perform site visits, support recruitment strategies, train site staff, and ensure regulatory compliance across TMF/ISF documentation.
We value strong communication, collaboration with study teams, and a minimum of 2 years on-site monitoring experience. The role requires full UK right to work and offers a dynamic, career-forward path with
The Onsite Clinical Research Associate - GCP/ICH Expert role at Iqvia Uk's Cfsp is now open for applications in England, United Kingdom.
Are you ready to take on the Onsite Clinical Research Associate - GCP/ICH Expert role at Iqvia Uk's Cfsp?
We would love to welcome a new Onsite Clinical Research Associate - GCP/ICH Expert to our group in England, United Kingdom.
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