IQVIA in the United Kingdom seeks experienced Clinical Research Associates to monitor trials and ensure sites conduct studies according to the protocol and regulatory requirements. The role involves site visits, recruitment tracking, protocol training, TMF/ISF maintenance, data query resolution, and collaboration with the study team to ensure quality and timely delivery.
Applicants should have a Bachelor's degree in a scientific discipline or healthcare, at least 1 year of on-site monitoring
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Clinical Research Associate II: Site Monitoring & Studies in Reading 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.
