IQVIA is seeking experienced Clinical Research Associates to join our Site Management team in the UK. The role involves performing site monitoring visits, ensuring regulatory compliance and data integrity, and coordinating with investigative sites to support study timelines.
You will administer protocol training, track submissions and recruitment, and maintain essential TMF/ISF records while collaborating with the study team to manage expectations and issues.
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Clinical Research Associate II: Flexible Work & Growth in Manchester 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.
