Informed Consent Specialist II, China, office based

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.

We are currently seeking an Informed Consent Specialist II to join our diverse and dynamic team. As an Informed Consent Specialist II at ICON, you will take a lead role in the development, review, and oversight of informed consent documents for complex, global clinical trials. You will act as a subject matter expert, ensuring that consent materials are ethically sound, compliant, and understandable to participants.

**What You Will Be Doing:**

+ Leading the creation, review, and optimisation of global and local informed consent forms (ICFs) in alignment with protocol, regulatory, and sponsor requirements.
+ Advising study teams on informed co...