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ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. In this role, you will be responsible for quality checking source documents against Good Documentation Practices and study protocols, performing data entry from source documents into the Case Report Form database, and organizing and maintaining subject charts for review by clinic staff and other study team members. You will also communicate identified errors and support clinic staff to resolve them in a timely manner, collaborate with study team members to navigate data quality issues, and may assist with developing new work methods for data entry and QC of study documentation.