Study Lead Programmer (Quilmes)

Study Lead Programmer - Argentina
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. 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.

What You Will Do:

• Develop and validate SAS programs for statistical analysis and reporting of clinical trial data.
• Collaborate with biostatisticians to define analysis plans and statistical methods to be applied to clinical data.
• Perform quality control checks on statistical outputs and ensure accuracy and consistency in reporting.
• Assist in the preparation of statistical reports, presentations, and publications for regulatory submissions.
• Contribute to process improvements b...