Senior Informed Consent Lead — Global Clinical Trials

ICON plc is seeking a Senior Informed Consent Specialist to lead development and oversight of informed consent strategies for complex global clinical studies. You will ensure patient-facing materials are ethical, compliant, and understandable. In this role you will coordinate with sponsors, ethics committees, and regulatory authorities, oversee translation and version control, and mentor junior specialists to drive best practices across regions. J-18808-Ljbffr