IQVIA UK is seeking an experienced Clinical Research Associate for the South West England region. The role involves on-site monitoring visits, protocol training, and collaboration with study teams to ensure regulatory compliance and data integrity.
The candidate should have at least 2 years of independent on-site monitoring experience in interventional studies, with familiarity in start-up, enrolment, maintenance and close-out processes. UK right to work is required.
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Clinical Research Associate — Flexible Site Monitoring (UK) 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.
