Informed Consent Specialist II

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 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.

**What You Will Do:**

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

+ Leading the creation, review, and optimization of global and local informed consent forms (ICFs) in alignment with protocol, regulatory, and sponsor requirements.
+ Advising study teams on informed consent strategy, content, and country-specific considerations, including complex or high-ris...