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 global clinical development within a diverse, collaborative culture at ICON.
Annual leave entitlements
Health insurance offerings
General Employee Assistance Programme
Life assurance
Flexible country-specific optional benefits
Design, develop, and validate SAS programs for clinical trial data analysis
Collaborate with biostatisticians to shape analysis plans and methodologies
Conduct comprehensive quality control checks on statistical outputs
Contribute to statistical reports, presentations,



and regulatory submission documentation
Identify enhancements to programming processes and drive continuous improvement
Proven 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 xkdbapo 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
SAS programming
Statistical analysis of clinical trial data
Quality control and validation processes
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📌 Senior Statistical Programmer - Icon Clinical Plc (Barcelona)
🏢 Jobrapido
📍 Barcelona