Full-time

Study Lead Programmer

Posted by ICON Clinical Research • June 06, 2026

📍 Buenos Aires, Argentina, Argentina
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Description

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:**

You will lead on statistical programming tasks requiring technical depth, with a focus on quality and continuous improvement.

Key responsibilities include:

+ 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 ...

Ready to Seal the Deal?

Submit your application today and take the next step in your career with ICON Clinical Research.

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