IQVIA in the United Kingdom is seeking experienced Clinical Research Associates to monitor and manage sites, ensuring studies comply with the protocol, regulations, and sponsor requirements. You will perform site visits, support recruitment plans, and maintain study documentation across multiple trials.
The role requires on-site monitoring experience, strong knowledge of GCP/ICH guidelines, and excellent communication, time management, and collaboration skills.
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Senior CRA II: On-site Monitoring & Site Management (UK) in Livingston 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.
