Teams at ICON plc

Lead and conduct clinical trial monitoring to ensure protocol and GCP compliance. Perform site visits, resolve issues, support data quality, train site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships to ensure timely trial execution. Role is sponsor-dedicated and based in the GTA with ~60% travel.

Manage site start-up and activation tasks for assigned clinical trial sites, including collection and review of essential documents, eTMF accuracy, ICD/ICF review, tracking actions and timelines, escalating delays, and collaborating with CROs and internal teams to improve site activation metrics and resolve issues.

Lead design, deployment and management of eCOA/ePRO systems for decentralized trials. Serve as sponsor SME and project manager, define requirements, oversee UAT, vendor selection and oversight, resolve system issues, integrate eCOA data with CTMS and data warehouses, ensure documentation and audit readiness, provide training, and coordinate cross-functional delivery within timelines and budgets.