IQVIA UK ‘s Site Management (multi-sponsor) team is growing and seeking junior and experienced Clinical Research Associates. You will perform site monitoring visits, adapt recruitment plans, and train sites on protocols to ensure study integrity and regulatory compliance.
The role requires independence in monitoring, strong knowledge of GCP/ICH, and willingness to travel to diverse investigative sites.
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CRA2: Site Monitoring Specialist — Clinical Trials 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.
