IQVIA UK is seeking a Senior Clinical Research Associate with Phase 1 experience to join the cFSP team in London. You will perform site monitoring visits and ensure GCP/ICH compliance while coordinating with sites to support study conduct.
4+ years of on-site monitoring in interventional trials, valid UK right to work, and strong collaboration are essential. IQVIA offers development opportunities and flexible work arrangements to help deliver patient outcomes.
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Senior CRA – Phase 1 Monitoring (Flexible Work) 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.
