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# Statistical Programmer

- **Company:** ICON plc
- **Location:** UK (Remote available)
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Clinical Data Management, Computer Programming, Data Integrity, SAS (Software), Data Processing, Information Technology
- **Published:** October 22, 2026
- **Apply:** https://dejobs.org/x/x/4CCA19EBAE2E4412880113BF35DD2400/job/

## About the Role

* Bachelor's degree in statistics, computer science, mathematics, or a related discipline
 * Proven experience as a statistical programmer within the clinical research industry, with strong knowledge of statistical methodologies and programming.
 * Proficiency in programming languages such as SAS, with experience in clinical data management systems.
 * Strong analytical and problem-solving skills, with a keen attention to detail and the ability to work independently.
 * Excellent communication skills, with the ability to convey complex statistical concepts to non-technical stakeholders and collaborate effectively with team members.

## Description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Statistical Programmer at ICON, you will the development, validation, and execution of statistical programs to support clinical trial analysis and reporting. You will be working with as part of a team dedicated to a globally recognised client in the medical devices space.

What You Will Do:

You will contribute to statistical programming activities, taking responsibility for your deliverables and working collaboratively., * Developing, validating, and maintaining complex statistical programs (SAS) for data manipulation, analysis, and reporting in clinical trials.

 * Collaborating with biostatisticians and cross-functional teams to interpret study requirements and ensure the accurate implementation of statistical analyses.
 * Preparing and reviewing statistical analysis plans (SAPs), programming specifications, and derived datasets to meet regulatory standards.
 * Ensuring data integrity and compliance with industry regulations, including ICH/GCP guidelines, throughout the programming process.
 * Mentoring junior programmers and assisting in training team members on programming techniques and best practices.