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:
Solid 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.
Solid 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
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