Position Summary

We are seeking an experienced Clinical SAS Programmer Lead to support Phase II–IV clinical studies and regulatory submissions. The ideal candidate will possess strong expertise in SAS programming, CDISC standards (SDTM/ADaM), TLF generation, and clinical trial data analysis. This role involves leading programming activities, collaborating with cross-functional teams and clients, mentoring junior programmers, and ensuring high-quality regulatory deliverables within project timelines.

Key Responsibilities

• Lead programming activities for Phase II–IV clinical studies of simple to moderate complexity.
• Develop, validate, and maintain SAS programs for data extraction, transformation, analysis, and reporting.
• Generate and validate Tables, Listings, and Figures (TLFs) for clinical and safety reporting.
• Create, validate, and deliver CDISC-compliant SDTM, ADaM, Define.xml, and aCRF deliverables.
• Analyze and integrat...