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Clinical Research Associate — Onsite Monitoring & Trials
Job Description & How to Apply Below
IQVIA in the UK is seeking an experienced Clinical Research Associate to monitor sites, ensure GCP compliance and data integrity across multiple protocols.
You will perform site visits, coordinate training, manage communications with study sites, and support regulatory submissions while traveling to assigned sites as needed. A life science degree and hands-on monitoring experience are required.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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