ICON Strategic Solutions is seeking an ICF Specialist based in the UK to lead the development, review, and oversight of informed consent documents for complex, global clinical trials.
You will work fully embedded within a growing Biotechnology partner, collaborating with internal teams and external partners to ensure accuracy, regulatory compliance and patient readability, while delivering timely reviews in a fast-paced environment.
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Global ICF Specialist – Patient-Focused Clinical Trials employer: ICON Strategic Solutions
ICON plc is an exceptional employer located in Reading, offering a dynamic work culture that prioritises quality and compliance in clinical trials. Employees benefit from competitive salaries, comprehensive benefits, and ample opportunities for professional growth through collaboration with cross-functional teams and participation in audits. The company's commitment to excellence and innovation makes it a rewarding place for those looking to make a meaningful impact in the field of clinical research.
