Website:
veramed.com
Job details:
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:
- 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.
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