Senior Clinical SAS Developer

Job Summary

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

Key Responsibilities

• Design, develop, and validate SAS macros to enhance clinical trial programming workflows
• Collaborate with biostatisticians and data managers to gather requirements and implement CDISC-compliant solutions
• Create documentation for macros and develop QC tools to ensure regulatory compliance

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 clinical trials or the pharmaceutical industry
• Proven experience in macro development using Base SAS and SAS Macro Language
• Strong knowledge of CDISC SDTM and ADaM standards
• Familiarity with clinical trial data structures and regulatory submission requirements