Overview In 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 integral clinical development within a diverse, collaborative culture at ICON.

Compensaciones / BeneficiosAnnual leave entitlementsHealth insurance offeringsCompetitive retirement planningGlobal Employee Assistance ProgrammeLife assuranceFlexible country-specific optional benefits ResponsabilidadesDesign, 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 improvement Requisitos 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

📌 Senior Statistical Programmer (Barcelona)
🏢 Jobrapido
📍 Barcelona