IQVIA UK is expanding its cFSP team and seeks experienced Clinical Research Associates to monitor interventional studies on-site in the UK. You will conduct site visits, manage recruitment plans and ensure protocol training and communications with sites are robust.
Role requires at least 2 years of on-site monitoring experience, strong GCP/ICH knowledge, and full UK right to work. The position offers growth within a globally leading clinical research organization.
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Experienced Clinical Research Associate — Flexible Work & Growth 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.
