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Job Description & How to Apply Below
IQVIA cFSP (sponsor‑dedicated) is seeking experienced Senior Clinical Research Associates in the UK. You will perform site monitoring to ensure sites conduct studies per protocol, regulations, and sponsor requirements, with oversight of data reporting and study progress.
Responsibilities include site visits, recruitment planning, protocol training, and maintaining TMF/ISF documentation while collaborating with study teams to support project execution and issue resolution.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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