IQVIA in the United Kingdom seeks experienced Clinical Research Associates for on-site monitoring roles across multiple sites. You will ensure sites conduct studies per protocol, manage data queries, and maintain study files in compliance with GCP and regulatory standards.
Responsibilities include site visits, recruitment tracking, and collaboration with the study team to meet project timelines. A science-based degree and 1+ year on-site monitoring experience are preferred.
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CRA II: UK Site Monitoring & Study Delivery 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.
