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The Senior Statistical Programmer is responsible for designing and validating SAS programs for clinical trial data analysis, mentoring junior staff, and ensuring regulatory compliance.

As an Epidemiologist, you will design studies, perform analyses, prepare reports, and support client engagement while ensuring compliance with policies.

The Senior TMF Specialist will support the clinical development mission of ICON plc, focusing on operational excellence and compliance throughout clinical trials.

Lead and mentor statistical programming teams, ensuring quality deliverables are met on time while supporting recruitment and operational activities.

The Data Analyst I will perform image data reconciliation, ensuring accuracy between EDC and image data, while collaborating with teams and maintaining compliance.

The Logistics Coordinator II will manage logistics activities for clinical trials, ensuring timely shipments while collaborating with cross-functional teams to meet compliance requirements.

The Pharmacovigilance Associate will monitor pharmaceutical safety by collecting and analyzing adverse event reports, ensuring regulatory compliance.

The Senior Pharmacovigilance Associate manages and oversees pharmacovigilance activities, ensuring regulatory compliance, analyzing safety data, and mentoring junior staff.

The Financial Analyst II will provide financial and consulting services, assist in reporting, forecasting, budgeting, and developing financial plans for support departments.

As an Intern, you will assist in validating clinical applications, collaborate with teams to resolve issues, and maintain documentation following GCP standards.