Senior Informed Consent Specialist

Job description

Senior Informed Consent Specialist ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development As a Senior Informed Consent Specialist at ICON, you will lead the development and oversight of informed consent strategies and documents for complex, global clinical studies. You will act as a subject matter expert, ensuring participant-facing materials are ethical, compliant, and understandable. What You Will Do: You will take ownership of scientific operations deliverables, applying your expertise to complex challenges. Key responsibilities include: Leading the creation, review, and optimisation of global and country-specific informed consent forms for complex or high-risk studies. Advising study teams on informed consent strategies, including readability, cultural considerations, and local regulatory expectations. Overseeing translation, localisation, and version control processes to ensure consistency and traceability across regions. Interacting with sponsors, ethics committees, and regul...