Jobs at ICON plc

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.

Oversee and monitor clinical trial sites to ensure GCP and protocol compliance, conduct site visits, resolve issues, ensure data integrity, train site staff and CRAs, collaborate with cross-functional teams, and maintain stakeholder relationships to support trial execution.

As a Global Study Manager, you will lead projects, manage cross-functional teams, and ensure successful project execution while mentoring team members.

Lead Clinical Data Science project teams to plan, set up, maintain and close clinical data systems. Provide technical review, support sales/bid defense, oversee system integration and vendor interactions, manage timelines/budgets, perform CRF and UAT peer review, and act as primary contact for internal and external stakeholders.