Senior Statistical Programmer - Icon Clinical Plc

Jobrapido; Barcelona; Presencial; EUR 55.000 - 75.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements

Health insurance offerings

Global Employee Assistance Programme

Life assurance

Flexible country-specific optional  bi

Descripción de la vacante

ICON is seeking a skilled SAS Programmer to design, implement, and validate SAS programs for clinical trial data analyses. You will collaborate with biostatisticians to shape analysis plans and ensure outputs meet regulatory standards.

You will perform thorough quality checks, contribute to statistical reports and regulatory submissions, and drive continuous improvement of programming processes within a diverse, collaborative culture in Barcelona, Spain.

Formación

• 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 or Master’s degree in Statistics, Mathematics, Computer Science or related discipline.

Responsabilidades

• Design, develop, and validate SAS programs for clinical trial data analyses.
• Collaborate with biostatisticians to shape analysis plans and methodologies.
• Perform 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.

Conocimientos

SAS programming

Statistical analysis

Clinical trial data

Quality control

Biostatistics

Communication

Educación

Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science

Herramientas

SAS

Descripción del empleo

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
• Global 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