ICON Strategic Solutions is recruiting an In Vivo Toxicology Manager (Study Monitor) for a 6-month fixed-term contract. This fully home-based UK role requires hands-on GLP toxicology experience, strong project management, and the ability to coordinate with CROs and internal teams to deliver high-quality regulatory studies.
As part of ICON’s global ecosystem, you will drive study design, execution, oversight and reporting, ensuring timelines and quality standards are met.
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Remote UK In Vivo Toxicology Study Monitor 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.
