Description
ICON is hiring a Clinical Study Manager to lead and coordinate central laboratory activities across global clinical studies. The role manages human biological samples, laboratory operations, sample chain of custody, vendor and partner relationships, budgets, performance reporting, and cross-functional stakeholder coordination. Candidates need a master’s degree in a relevant life or medical science discipline, at least five years of clinical laboratory and clinical trial experience, knowledge of ICH-GCP and GCLP, and strong project management and communication skills. The position is remote and requires the legal right to work in the country where the role is based.
