IQVIA UK’s Site Management team is seeking experienced Clinical Research Associates to monitor trials in accordance with GCP/ICH guidelines. This role involves independent on-site monitoring and managing multiple protocols across diverse investigative sites in the Manchester region.
You will train sites on protocol requirements, coordinate recruitment plans, and ensure regulatory submissions and TMF/ISF maintenance. Travel to sites is required as projects demand.
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Oncology CRA II: Lead Site Monitoring & Trials 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.
