
This senior clinical research associate role at ICON plc focuses on ophthalmology trials within a global healthcare intelligence organization. The position involves leading complex monitoring tasks to ensure sites adhere to protocols, regulatory standards, and Good Clinical Practice. Key responsibilities include conducting site visits to assess performance, collaborating with cross-functional teams for accurate data reporting, and providing mentorship to junior staff. The role appeals to professionals seeking a diverse, inclusive culture that rewards high performance and supports work-life balance through comprehensive benefits. While the position requires approximately 60% travel, it offers significant opportunities for professional growth and the chance to shape the future of clinical development.

















