Senior Clinical SAS Macro Developer

Job Summary

A company is looking for a Senior Clinical SAS Macro Developer Consultant.

Key Responsibilities

• Design, develop, and validate SAS macros to streamline clinical trial programming workflows
• Collaborate with biostatisticians and clinical programmers to implement solutions aligned with CDISC standards
• Create documentation for macros and support the deployment and maintenance of macro libraries

Required Qualifications

• Bachelor's or Master's degree in Computer Science, Statistics, Life Sciences, or a related field
• 5+ years of SAS programming experience in the clinical trials or pharmaceutical industry
• Proven experience in macro development using Base SAS and SAS Macro Language
• Strong working knowledge of CDISC SDTM and ADaM standards
• Experience with clinical trial data structures and regulatory submission requirements