Statistical Analyst

As a Statistical Analyst at ICON, you will play a crucial role in supporting clinical trial activities by contributing to study design, developing statistical analysis plans, and performing complex statistical programming. You will collaborate with cross-functional teams to ensure the timely delivery of high-quality data analysis and reporting, ultimately helping to bring new medicines to patients faster.

• Support clinical trial activities and study design
• Write statistical methods sections and analysis plans
• Program statistical procedures using SAS/Graph
• Develop complex macros and project deliverables
• 4+ years of statistical programming experience in pharma/biotech/CRO
• Proficiency in SAS and foundational knowledge of R

• Must be authorized to work without sponsorship.