Statistical Programmer I

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

At ICON, we’re looking for a Statistical Programmer I who is ready to do more than just write code, you will help bring clinical research to life. You will join a collaborative, diverse team working on studies that genuinely matter, where your expertise helps turn complex data into clear insights that shape medical advancements. If you enjoy solving problems, working closely with experts across disciplines, and seeing the tangible impact of your work, this could be the role for you.

About ICON

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.

At ICON, your work isn’t just technical, it’s meaningful.

Responsibilities

• Building impactful solutions – Develop, validate, and maintain complex statistical programs (primarily in R) to support data analysis and reporting for clinical trials.
• Leading from the front – Take ownership of one or more studies, working alongside Principal Programmers and acting as a key contact for a leading FSP sponsor.
• Collaborating across teams – Partner closely with biostatisticians and cross-functional colleagues to translate study requirements into robust, accurate statistical outputs.
• Shaping analysis strategy – Prepare and review statistical analysis plans (SAPs), programming specs, and derived datasets to meet regulatory expectations.
• Ensuring quality and compliance – Safeguard data integrity and adhere to industry standards (ICH/GCP) throughout the programming lifecycle.
• Supporting others to grow – Mentor junior programmers and contribute to building a culture of knowledge-sharing and continuous improvement.

Requirements

• You Bring A degree in statistics, mathematics, computer science, or a related field (postgraduate qualifications are a bonus).
• 1+ year of experience as a statistical programmer within clinical research.
• Hands-on experience in R programming (ideally 1+ years in a clinical trials setting).
• A sharp analytical mindset, attention to detail, and confidence working independently.
• The ability to explain complex statistical concepts in a clear, accessible way—and collaborate effectively with both technical and non-technical stakeholders.

Why ICON?

• You’ll contribute to research that improves lives, while working in an environment that values collaboration, innovation, and growth.
• Whether you’re leading studies or mentoring others, you’ll have the support and autonomy to make a real difference.
• Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Benefits

• ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage

Employee assistance programmes and wellbeing resources

• Learning and development opportunities through structured training and career pathways
• Benefits may vary depending on role and location.
• Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here . Are you a current ICON Employee? Please click here to apply