Senior SAS Programmer for Clinical Trials & Insights

Icon Clinical Plc; Madrid; Presencial; EUR 60.000 - 90.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Pension plans

Life assurance and disability coverage

Employee assistance programmes andWell

Wellbeing resources

Learning and development opportunities

Descripción de la vacante

ICON Clinical Plc is seeking a Senior Statistical Programmer in Madrid, Spain, to develop and validate SAS programs for clinical trials. You will work with biostatisticians to shape analysis plans and deliver high-quality, regulatory-ready outputs.

The role emphasizes collaboration, attention to detail, and a proactive approach to process improvement within a supportive, global team. Employment requires a relevant degree and experience in clinical research or pharma, with strong communication

Formación

• Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or related discipline.
• Proven experience in statistical programming, ideally within clinical research or the pharmaceutical industry.
• Strong command of SAS programming and statistical concepts.
• Excellent analytical and problem-solving abilities.

Responsabilidades

• Designing, developing, and validating SAS programs to support statistical analysis and reporting of clinical trial data.
• Collaborating with biostatisticians to shape analysis plans, identify appropriate methodologies, and deliver reliable insights.
• Conducting comprehensive quality control checks to ensure the accuracy, consistency, and integrity of statistical outputs.
• Supporting the creation of statistical reports, presentations, and regulatory submission documentation.
• Identifying opportunities to enhance programming processes, contributing to continuous improvement and innovation within the team.

Educación

Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or related discipline

Herramientas

SAS

Descripción del empleo

ICON Clinical Plc is seeking a Senior Statistical Programmer in Madrid, Spain, to develop and validate SAS programs for clinical trials. You will work with biostatisticians to shape analysis plans and deliver high-quality, regulatory-ready outputs.

The role emphasizes collaboration, attention to detail, and a proactive approach to process improvement within a supportive, global team. Employment requires a relevant degree and experience in clinical research or pharma, with strong communication