IQVIA UK’s RWE team is seeking a Clinical Research Associate II to support Phase 3b and Phase 4 studies across a diverse range of therapeutic areas. The CRA will cover sites across UK & Ireland, with 6-7 site visits per month.
Responsibilities include site monitoring visits, site training, and ensuring regulatory compliance. The role requires 1–2 years on-site monitoring experience, a degree in a scientific or health discipline, and strong knowledge of GCP/ICH guidelines.
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CRA II: UK & Ireland Clinical Trials Monitor (Phase 3/4) 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.
