ICON plc is seeking a Clinical Research Associate to help advance clinical research and bring new therapies closer to patients. In this role, you will coordinate and monitor clinical trial sites, verify source documentation and data quality, and ensure studies follow approved protocols, Good Clinical Practice, and applicable regulations. You will work closely with investigators, site teams, sponsors, and global study colleagues to resolve issues, track milestones, and protect participant safety. The work calls for strong organization, clear communication, sound judgment, and attention to detail in a fast-paced, quality-focused environment. Join a collaborative, patient-focused organization committed to scientific excellence, integrity, innovation, and continuous learning, with opportunities to grow while contributing to meaningful clinical research outcomes worldwide.
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