ICON Plc is seeking a Senior CRA to oversee clinical trial monitoring and ensure adherence to protocols, regulatory requirements and GCP standards. The role involves leading monitoring tasks, site visits, and collaboration with cross-functional teams to ensure accurate data collection and reporting.
You will train site staff, manage multiple sites, and build strong relationships with investigators and stakeholders, with travel as required within the country to support trial execution.
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Sr. CRA II — Lead Monitoring & Training 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.
