We are seeking an experienced Statistical Programmer with 8 OR 8 years of experience in clinical trials and pharmaceutical research The ideal candidate should possess strong expertise in SAS programming and clinical data standards including SDTM ADaM and TFL development Key Responsibilities Develop and validate SDTM and ADaM datasets as per CDISC standards Generate Tables Listings and Figures TLF TFL for clinical study reports Perform SAS programming for clinical trial data analysis and reporting Collaborate with Biostatisticians Data Management and Clinical Operations teams Review protocol SAP CRF and data specifications Ensure compliance with regulatory requirements and industry standards Perform quality checks and validation of programming outputs Support regulatory submissions and audits when required Required Skills 8 years of Statistical Programming experience Robust SAS Programming skills Handson experience with SDTM ADaM and TFL TLF development Knowledge of CDISC standards and clinical trial processes Experience in pharmaceutical biotechnology or CRO environments Exposure to regulatory submissions FDA EMA PMDA is preferred Strong analytical and problemsolving skills

📌 Senior Programmer Analyst II Statistical programmer (Bengaluru)
🏢 American Express
📍 Bengaluru