ICON Clinical Research is seeking a Senior Clinical Research Associate (CRA) to oversee and manage clinical trial activities within the Full-Service team in the UK. The role focuses on data integrity, regulatory compliance, and patient safety across multiple sites and study lifecycles.
The Senior CRA will monitor sites, conduct visits, collaborate with cross-functional teams, and provide training to site staff to ensure high standards of trial conduct and timely data reporting.
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Senior Clinical Research Associate β Full-Service CRA in Reading employer: ICON Clinical Research
At ICON plc, we pride ourselves on being a world-leading healthcare intelligence and clinical research organization that champions innovation and excellence. As a Senior Director in Regulatory Affairs, you will thrive in our inclusive culture that prioritises employee growth and well-being, offering competitive benefits such as flexible leave, comprehensive health insurance, and a supportive work-life balance. Join us in shaping the future of clinical development while enjoying a dynamic environment that fosters collaboration and professional development.