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# Senior Sas Programmer I

- **Company:** Icon Clinical PLC
- **Location:** Barcelona, Spain
- **Contract:** Permanent contract
- **Skills:** Clinical Data Repository, SAS (Software), Information Technology
- **Published:** August 24, 2026
- **Apply:** https://www.buscojobs.com.es/senior-sas-programmer-i-en-barcelona-ID-368520730

## About the Role

What You Will Be DoingDesigning, developing, and validating SAS programs to support statistical analysis and reporting of clinical trial data.Collaborating with biostatisticians to shape analysis plans, identify appropriate methodologies, and deliver reliable insights.Conducting comprehensive quality control checks to ensure the accuracy, consistency, and integrity of statistical outputs.Your ProfileBachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a related discipline.Strong command of SAS programming, with a solid grounding in statistical concepts and clinical data analysis.Effective communicator with strong teamwork skills and the confidence to translate complex analyses into clear, actionable insights.Employment with ICON is contingent upon having the legal right to work in the country where the role is based.Competitive base salary and performance related incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where
applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.Czech Republic, Prague; KenyaType: Full time

## Description

Senior Statistical Programmer - Client BasedICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.We're looking for a talented Senior Statistical Programmer to become a key contributor within our diverse, collaborative, and forward?thinking team.At ICON, you'll play an integral role in transforming clinical trial data into meaningful insights that drive critical decision?making in global healthcare.In this role, you'll take ownership of developing and validating high?quality statistical programs, partnering closely with expert biostatisticians, and ensuring our outputs meet the highest scientific and regulatory standards.What You Will Be DoingDesigning, developing, and validating SAS programs to support statistical analysis and reporting of clinical trial data.Collaborating with biostatisticians to shape analysis plans, identify appropriate methodologies, and deliver reliable insights.Conducting comprehensive quality control checks to ensure the accuracy, consistency, and integrity of statistical outputs.Your ProfileBachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a related discipline.Strong command of SAS programming, with a solid grounding in statistical concepts and clinical data analysis.Effective communicator with strong teamwork skills and the confidence to translate complex analyses into clear, actionable insights.Employment with ICON is contingent upon having the legal right to work in the country where the role is based.Competitive base salary and performance related incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.Czech Republic, Prague; KenyaType: Full time


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