Senior Study Lead Programmer — Clinical Trials (Río Cuarto) (Argentina)
Icon Strategic Solutions • , , argentina, , , argentina • Posted June 17, 2026
About the Role
What You Will Do:
As a Senior Statistical Programmer I at ICON, you will analyse clinical trial data and support the statistical analysis process to ensure high-quality results.
Key Responsibilities:
- Developing and validating SAS programs for statistical analysis and reporting of clinical trial data.
- Collaborating with biostatisticians to define analysis plans and statistical methods to be applied to clinical data.
- Performing quality control checks on statistical outputs and ensuring accuracy and consistency in reporting.
- Assisting in the preparation of statistical reports, presentations, and publications for regulatory submissions.
- Contributing to process improvements by identifying efficiencies in programming practices and methodologies.
Your Profile:
You will have a strong foundation in statistical programming, with the experience to work independently and guide others.