Statistical Programmer II

About the role

As a Statistical Programmer II at ICON, you will the development, validation, and execution of statistical programs to support clinical trial analysis and reporting.

What you'll do

• Developing, validating, and maintaining complex statistical programs (SAS, R, or similar) for data manipulation, analysis
• Collaborating with biostatisticians and cross-functional teams to interpret study requirements and ensure the accurate implementation of statistical analyses
• Preparing and reviewing statistical analysis plans (SAPs), programming specifications, and derived datasets to meet regulatory standards
• Ensuring data integrity and compliance with industry regulations, including ICH/GCP guidelines, throughout the programming process
• Mentoring junior programmers and assisting in training team members on programming techniques and best practices

What you need

• 2–5 yrs of experience
• SAS
• Clinical research
• R
• CRO
• Learning and development
• Communication
• Any graduate