IQVIA UK is seeking an experienced Clinical Research Associate for the cFSP sponsor-dedicated team. You will perform site monitoring visits, manage recruitment plans, and ensure regulatory compliance while maintaining regular communication with sites.
The role requires at least 2 years of on-site monitoring experience in interventional studies, a degree in a scientific discipline or healthcare, and full UK work entitlement. Visa sponsorship is not offered.
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Clinical Research Associate II - On-Site Monitoring in Reading employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South West England location provides flexible working arrangements, comprehensive well-being support, and robust career development opportunities through our AI-powered talent marketplace, ensuring that you can thrive both personally and professionally while contributing to meaningful advancements in healthcare.
