IQVIA UK’s cFSP team is seeking a Senior Clinical Research Associate with Phase 1 monitoring experience to support site visits and trial management. You will perform site monitoring visits, drive recruitment plans, and ensure GCP/ICH compliance while collaborating with study teams to resolve issues and maintain TMF/docs.
The role requires at least four years of on‑site monitoring experience and full UK right to work.
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Senior Phase 1 CRA — Flexible Work & Growth 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.
