Location: Pan India (Onsite)

Experience: 5–12 Years

We are hiring for a leading global organization and seeking experienced Statistical Programmers with strong expertise in clinical trial data analysis, programming, and regulatory submissions.

Key Responsibilities

• Develop, validate, and maintain statistical programming deliverables for clinical studies.
• Create and validate SDTM and ADaM datasets in compliance with CDISC standards.
• Generate and validate Tables, Listings, and Figures (TLFs) for clinical study reports.
• Prepare and support submission deliverables including Define.xml , Reviewer Guides, and related documentation.
• Develop and maintain SAS programs, macros, and validation processes .
• Utilize R programming for statistical analysis, data visualization, and reporting.
• Support regulato...