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Clinical Research Associate: Site Monitoring & Management
Job Description & How to Apply Below
IQVIA cFSP (sponsor-dedicated) seeks experienced Clinical Research Associates in the UK to ensure sites conduct studies per protocol, regulations, and sponsor requirements.
Responsibilities include site monitoring visits, site training, recruitment planning, and TMF/ISF maintenance, with collaboration across study teams and potential start-up support. Requires at least 1 year of on-site monitoring experience and strong English communication.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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