Statistical Programmer II

Statistical Programmer II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

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 Will Do:

• Developing, validating, and maintaining complex statistical programs (SAS, R, or similar) for data manipulation, analysis, and reporting in phase IV trials and peri/post approval studies
• 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.

Your Profile:

• 2+ years of statistical programming experience within the pharmaceutical, biotechnology, or CRO industry.
• Strong hands-on expertise in SAS programming, with experience supporting clinical trial deliverables and statistical analyses.