Senior Statistical Programmer/Analyst Consultant (Cardiovascular, Renal)
Related skills
sas cdisc sdtm adam tlfs📋 Description
- Lead or support programming tasks to deliver components of a project
- Develop, validate SAS programs for study data analysis and reporting
- Create datasets, tables, listings, and figures per study needs
- Collaborate with Biostatistics, Data Management, and Clinical teams
- Ensure programming deliverables meet quality and timelines
- Support study planning, specifications, and submissions
🎯 Requirements
- Strong SAS programming in pharmaceutical/CRO settings
- Hands-on CVRM experience (Cardiovascular, Renal & Metabolism)
- SDTM, ADaM, and TLFs generation and validation
- Knowledge of CDISC standards and clinical trial processes
- Independent work style; able to manage multiple priorities
- Regulatory submissions experience preferred
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