Lead the creation and validation of advanced SAS programs that support statistical analysis, data reporting, and critical decision‑making across clinical studies
Job Summary
Lead the creation and validation of advanced SAS programs that support statistical analysis, data reporting, and critical decision‑making across clinical studies.
Partner closely with biostatisticians to translate scientific objectives into robust analysis plans and ensure the right methodologies are applied.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
Matching Summary
Lead the creation and validation of advanced SAS programs that support statistical analysis, data reporting, and critical decision‑making across clinical studies.
Skills & Requirements
Must-have
SAS programming expert
statistical analysis
data reporting
regulatory submissions
quality control
clinical trial data structures
Nice-to-have
technical excellence
fresh thinking
leadership
collaborative environment
complex analytical challenges
multidisciplinary environment
Key Requirements
Bachelor's or Master's degree
Extensive statistical programmer experience
Pharmaceutical/biotech/clinical research industry experience