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 regulatory submissions to global health authorities including FDA and EMA . Collaborate closely with Biostatistics, Data Management, Clinical Operations, and Regulatory teams. Ensure adherence to industry s...