Teams at ICON plc

Conduct site selection, initiation, monitoring, and close-out visits for clinical trials across therapeutic areas. Ensure ICH-GCP and regulatory compliance, maintain CTMS and eTMF documentation, monitor patient safety and drug accountability, support recruitment and data quality, resolve issues, track budgets, and collaborate with clinical teams. The role requires 60%–75% travel for on-site monitoring visits.

Leads the strategic and tactical management of an Imaging Project Management team within clinical research. Responsibilities include supervising project managers and assistants, allocating resources, managing workloads and forecasts, developing performance metrics, resolving escalations, improving processes, overseeing training and compliance, supporting recruitment, managing financial performance, and leading risk and contingency planning. Requires up to 25% travel.

Manage feasibility and site activation activities for clinical studies, including project plans, timelines, site recommendations, regulatory and ethics submissions, essential documents, contracts, and activation milestones. Coordinate cross-functional and sponsor stakeholders, track KPIs, mitigate risks, resolve study issues, support audits and inspections, and ensure quality, budget, and timeline compliance. The role also includes mentoring, process improvement, business development support, and approximately 10% domestic or international travel.