Senior SAS Programmer: Clinical Trials Impact

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

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.