Teams at ICON plc

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.

Lead feasibility informatics strategy for clinical trial proposals and awarded feasibility projects. Provide data-driven feasibility analyses using internal/external data, support bid defenses, manage delivery and handover to site identification, assess risks, and collaborate with cross-functional teams to meet sponsor objectives.

The Senior Clinical Research Associate will manage site activities and ensure compliance during Oncology clinical trials, focusing on data integrity and subject safety.