Sr. Statistical Programmer

About the role

As a Senior Statistical Programmer, you will play a key role in transforming clinical trial data into accurate, meaningful statistical outputs that support medical research and drug development. You will develop, validate, and maintain complex statistical programs to generate tables, listings, figures, and analysis datasets.

What you'll do

• Develop and maintain statistical programming code using SAS or other relevant software to generate summary tables, data listings, graphs
• Perform independent validation programming and quality control activities to ensure the accuracy, consistency, and reliability of statistical outputs
• Review and interpret study documentation, including Statistical Analysis Plans, mock shells, annotated Case Report Forms (CRFs), programming specifications
• Lead statistical programming activities across assigned clinical projects, coordinating deliverables, monitoring progress
• Develop programming specifications for datasets and outputs of varying complexity, anticipating technical challenges and establishing efficient programming approaches

What you need

• 6–10 years in pharma & medical sales
• Clinical research
• SAS
• Documentation
• SOP writing
• Quality control
• Communication
• Any graduate