IQVIA UK Site Management team is expanding to include junior and experienced Clinical Research Associates to monitor trials across multiple sponsors. You will visit sites for initiation, monitoring, and close-out, ensuring GCP/ICH compliance and robust communication with sites.
The role involves supporting recruitment planning, protocol training, and continuous quality assessments while traveling to clinical sites as required.
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CRA2: Multi-Sponsor Site Monitoring (Travel) 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.
