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 valuable 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:





- Strong 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 (Neurology) (Bengaluru)
🏢 Veramed
📍 Bengaluru