Experienced Principal Statistical Programmer

Location:
Bangalore/Hyderabad/Remote Experience Required: 10+ years of Statistical Programming experience

Key Responsibilities
• Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs
• Author, review and approve study TFL shells and dataset specifications
• Author, validate and document SAS programs for datasets, TFLs and macros, applying good programming practice
• Identify data issues and outliers
• Complete, review and approve CDISC Validation tool reports
• Identify data and standards issues and resolve or escalate as appropriate
• Awareness of emerging standards and associated impact to ongoing and future planned trials
• Maintain proficiency in SAS and awareness of developments
• Maintain study master file documents and any other documents that are required to be audit ready. Required

Qualifications:




• Robust expertise in Base SAS and Advanced SAS Programming.
• Deep understanding of SAS Macro Language, including advanced macro development techniques.
• Extensive experience with PROC SQL, data integration, and complex data joins.
• Proven experience developing validation programs, test cases, and quality control documentation.
• Experience reviewing technical specifications, requirements documents, and programming deliverables.
• Excellent troubleshooting, debugging, and performance optimization skills.
• Strong communication and collaboration skills with the ability to work effectively with developers, statisticians, and clinical teams.
• Ability to independently analyze requirements and design scalable programming solutions.

📌 Principal Statistical Programmer (Bengaluru)
🏢 Veramed
📍 Bengaluru