Statistical Programmer II
On-site · Warsaw, Mazovia, Poland or Budapest, Budapest, Hungary
Job Summary
Develop, validate, and maintain complex statistical programs (primarily in R) to support data analysis and reporting for clinical trials. Take ownership of one or more studies, collaborating with Principal Programmers and acting as a key contact for a leading FSP sponsor. Partner with biostatisticians and cross-functional colleagues to translate study requirements into robust, accurate statistical outputs. Prepare and review statistical analysis plans (SAPs), programming specs, and derived datasets to meet regulatory expectations. Safeguard data integrity and adhere to industry standards (ICH/GCP) throughout the programming lifecycle. Mentor junior programmers and contribute to building a culture of knowledge-sharing and continuous improvement. Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Required Qualifications
- A degree in statistics, mathematics, computer science, or a related field (postgraduate qualifications are a bonus)
- Solid experience as a statistical programmer within clinical research
- Strong hands-on expertise in R programming (ideally 3+ years in a clinical trials setting)
- Ability to explain complex statistical concepts clearly and collaborate with stakeholders
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