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# Senior Statistical Programmer

- **Company:** Icon Clinical PLC
- **Location:** Barcelona, Spain
- **Contract:** Permanent contract
- **Skills:** Clinical Data Management, Clinical Data Repository, SAS (Software), Information Technology
- **Published:** September 19, 2026
- **Apply:** https://www.buscojobs.com.es/senior-statistical-programmer-en-barcelona-ID-372161992

## About the Role

Requisitos principalesProven experience in statistical programming, ideally in clinical research or pharmaceutical industry
Strong command of SAS programming and solid understanding of statistical concepts and clinical data analysis
Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or related discipline
Excellent analytical and problem-solving abilities with meticulous attention to detail
Effective communicator with strong teamwork skills and ability to translate complex analyses into clear insights
Effective communication
Team collaboration
Attention to detail
SAS programming
Statistical analysis of clinical trial data
Quality control and validation processes

## Description

OverviewIn this role you will design, implement, and validate SAS programs to support statistical analyses in clinical trials.You will work closely with biostatisticians to shape analysis plans and ensure outputs meet scientific and regulatory standards.You will perform thorough quality checks and help prepare statistical reports and regulatory submissions.You will look for opportunities to improve programming processes and contribute to team innovation.This is an opportunity to impact global clinical development within a diverse, collaborative culture at ICON.Compensaciones / BeneficiosAnnual leave entitlementsHealth insurance offeringsCompetitive retirement planningGlobal Employee Assistance ProgrammeLife assuranceFlexible country-specific optional benefitsResponsabilidadesDesign, develop, and validate SAS programs for clinical trial data analysisCollaborate with biostatisticians to shape analysis plans and methodologiesConduct comprehensive quality control checks on statistical outputsContribute to statistical reports, presentations, and regulatory submission documentationIdentify enhancements to programming processes and drive continuous improvementRequisitos principalesProven experience in statistical programming, ideally in clinical research or pharmaceutical industryStrong command of SAS programming and solid understanding of statistical concepts and clinical data analysisBachelor's or Master's degree in Statistics, Mathematics, Computer Science, or related disciplineExcellent analytical and problem-solving abilities with meticulous attention to detailEffective communicator with strong teamwork skills and ability to translate complex analyses into clear insightsEffective communicationTeam collaborationAttention to detailSAS programmingStatistical analysis of clinical trial dataQuality control and validation processes


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