Teams at ICON plc

Lead coordination and oversight of clinical trial activities to ensure protocol adherence, regulatory compliance, site management, data integrity, risk identification, and cross-functional collaboration to support study execution and continuous improvement.

Coordinate site activations and maintenance across studies; collect and review Critical Document Packages (CDPs); forecast activation dates; liaise with sites, sponsors, and internal stakeholders; ensure regulatory/IRB submissions and TMF quality; manage translations, CTAs/budgets support, escalate issues, and mentor team members while driving process improvements and KPI achievement.

The Senior Clinical Research Associate will monitor clinical studies compliance and conduct, ensuring adherence to protocols and regulations. Responsibilities include overseeing trials at sites and preparing reports.