Found Description
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
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