Teams at ICON plc

Facilitates clinical trial site activation by preparing regulatory and ethics submissions, coordinating approvals, maintaining submission records, supporting study document development, and contributing to start-up meetings. The role requires collaboration with internal and external stakeholders, strong organization, attention to detail, and the ability to manage multiple tasks independently in a fast-paced environment.

Oversee and coordinate oncology clinical trials, ensuring protocol adherence, regulatory compliance, data integrity, quality, and timely execution. Manage site activities, collaborate with cross-functional teams and investigators, support clinical staff, monitor trial progress, identify risks, and implement mitigation strategies. The role requires independent work, strong organization, and effective stakeholder communication.

Lead the development, validation, and maintenance of clinical data programming solutions for EDC/CDMS systems, vendor data, analytics, reports, integrations, and data transfers. Provide technical leadership across studies, serve as a programming subject matter expert, mentor programmers, support study teams, and drive automation and process improvements. Collaborate with data managers, biostatisticians, and project managers to ensure high-quality clinical trial data management solutions.