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Clinical Research Associate II Onsite Monitoring & Study Execution
Job Description & How to Apply Below
IQVIA UK is seeking experienced Clinical Research Associates to join the cFSP sponsor-dedicated team. You will perform site monitoring visits in line with GCP/ICH, support site recruitment, and manage study documentation and communications.
This role requires on-site work in the UK, with a minimum of 2 years of monitoring experience and the ability to collaborate with study teams and sites. IQVIA is committed to integrity and career development.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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