ICON Strategic Solutions is seeking an ICF Specialist based in the UK to lead development, review, and oversight of informed consent documents for complex global trials. The role embeds within a Biotechnology company, delivering high-quality ICF reviews and coordinating with internal and external stakeholders.
You will apply plain language principles, ensure regulatory compliance, and manage multiple priorities to meet study timelines while supporting related R&D initiatives.
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ICF Specialist - Global Clinical Trials Lead (UK/EU) 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.
