Clinical Trials Medical Writer - Informed Consent

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re committed to advancing clinical development and shaping the future of therapies. As an Informed Consent Writer, you will develop and prepare clinical trial documents, regulatory submissions, and scientific publications to support the progress of innovative treatments. You’ll collaborate with cross‑functional teams to write and edit CSRs, protocols, IBs, and patient narratives, perform literature #J-18808-Ljbffr ICON