ICON plc is a world-leading healthcare intelligence and clinical research organization. The Clinical Scientist will assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies, including adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management. This role may involve supporting a single study or multiple studies, or even leading a study with limited scope (e.g., Survival Follow-up). The Clinical Scientist will also interact with internal and external stakeholders such as study sites and committees to support clinical study objectives. ICON is committed to fostering an inclusive environment, driving innovation and excellence, and shaping the future of clinical development. The company is an award-winning workplace dedicated to making a difference in patients' lives by delivering new medicines and medical devices, while also conducting business sustainably and supporting local communities.
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Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees