Teams at ICON plc

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.

The Senior Clinical Research Associate monitors clinical studies, ensuring they comply with protocols and regulations while documenting progress both on-site and remotely.

Serve as primary contact between investigational sites and sponsor; perform site selection, initiation, routine monitoring, and close-out; ensure ICH‑GCP and Health Canada compliance; maintain CTMS/eTMF documentation; monitor safety reporting (AE/SAE/PQC); support recruitment, drug accountability, data query resolution, site budgets/payments, and escalate risks to the clinical team.