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Clinical Research Associate - Multi-Sponsor Site Monitoring
Job Description & How to Apply Below
IQVIA UK’s Site Management team is expanding, seeking junior and experienced Clinical Research Associates to monitor sites across multi-sponsor studies, ensuring compliance with GCP/ICH and trial protocols.
You will work with sites to drive recruitment, train staff, manage documentation such as TMF/ISF, and collaborate with the study team to keep trials on track and within regulatory requirements. Travel to sites is required, and strong communication with investigators is essential.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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