ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

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...