Teams at ICON plc

Conducts independent clinical study start-up, monitoring, documentation, regulatory submissions, and site close-out for Phase I–III/IV trials. Ensures compliance with ICH-GCP and applicable regulations, reviews medical data, manages sponsor queries and study costs, and may train fellow CRAs. Requires frequent international and domestic travel, including driving.

Leads cross-functional project and program delivery from initiation through completion, managing plans, timelines, budgets, resources, risks, stakeholders, reporting, and quality. Coordinates teams, resolves issues, monitors performance, communicates progress to senior management, and supports team capability development and continuous improvement. The role requires strong leadership, organization, communication, adaptability, and approximately 30% travel.

Prepare and execute invoicing and reporting for assigned accounts; negotiate site contracts, budgets, payment terms, ancillary agreements and amendments; partner with Study Startup, CROs and Clinical Operations to improve SB&C metrics; apply standards, use industry tools and data to provide budget and contract feedback aligned with fair market value; track negotiations, escalate delays, and support resolution of site activation issues.