Senior SAS Programmer for Clinical Trials (Contract)

TOTAL TRIALS INC; Centurion; On-site; ZAR 700,000 - 900,000; Full time

Job summary

Total Trials Inc. is seeking a Statistical Programmer to lead SAS programming for clinical projects. You will develop TFLs, analysis datasets, and reports with minimal guidance, ensuring data integrity and compliance with protocols and guidelines.

You will design SAS macros, maintain program documentation, and collaborate with biostatisticians to deliver timely analyses and accurate interpretations.

Qualifications

• Bachelor's degree in a quantitative field with statistical analysis.
• Minimum two years' SAS programming experience on research studies.
• Proficiency in SAS; knowledge of macro language is a plus.

Responsibilities

• Write statistical analysis programs using SAS for high-volume studies.
• Design and generate TFL shells and data set specifications from SP/SAP.
• Review analysis plans and study materials for accuracy.
• Coordinate with biostatisticians to provide study summaries.
• Create and document SAS macros and tools to improve efficiency.
• Prepare user documentation and train staff as needed.
• Support randomization programming and trial document filing.

Skills

SAS programming

SAS macro language

English communication

Attention to detail

Organizational skills

Problem solving

Independent work

Team collaboration

Statistical concepts

Programming standards

Education

Bachelor's degree in statistics/biostatistics

Tools

SAS

Job description

Total Trials Inc. is seeking a Statistical Programmer to lead SAS programming for clinical projects. You will develop TFLs, analysis datasets, and reports with minimal guidance, ensuring data integrity and compliance with protocols and guidelines.

You will design SAS macros, maintain program documentation, and collaborate with biostatisticians to deliver timely analyses and accurate interpretations.