Teams at ICON plc

Design and develop clinical data cleaning, reporting and visualization solutions (Elluminate) to support data validation, study status metrics and monitoring. Build reusable check libraries, collaborate with cross-functional teams on business rules, create/test listings and documentation, and improve reporting tools to ensure high-quality clinical trial data.

Support study start-up, site activation readiness, and maintenance tasks including ICF customization, translations, IRB/EC submissions, and eTMF documentation. Assist contract workflows and amendments, liaise with cross-functional teams, and work flexible hours to support global clinical trial operations.

Leads IT project and program management activities, including planning, scope definition, cross-functional implementation, stakeholder communication, documentation, reporting, and team mentoring. Develops project strategies, manages competing priorities, applies project management methodologies, and ensures successful delivery of IT initiatives. Requires experience leading projects in the pharmaceutical or biotech industry and willingness to travel approximately 1%.