Associate Principal Statistical Programmer
USD 144K-202K Mid-level Full Time
Tasks
- Build datasets tables listings and graphs
- Communicate programming progress with sponsor and resolve issues
- Create Define xml deliverables and support submission packages
- Create SDTM and ADaM programming specifications
- Develop and prioritize SAS macro development
- Develop execute and review SAS programs for clinical studies
- Ensure compliance with FDA PMDA and EMA submission standards
- Serve as SAS programming subject matter expert
- Support safety reporting patient data reviews and risk mitigation
- Validate safety efficacy and inferential results outputs
Perks/Benefits
Skills/Tech-stack
ADaM | Base SAS | CDISC | Clinical programming | Data Manipulation | Data Validation | Data review | Define-XML | Macro language | Patient data | Patient data review | Reporting Automation | Risk Mitigation | SAS | SAS Macro | SAS Macro Language | SAS Stat | SDTM | Safety reporting | TLF
Education
Bachelor of Arts | Bachelor of Engineering | Bachelor of Science | Bachelor of Science in Biostatistics | Bachelor of Science in Biotechnology | Bachelor of Science in Computer Science | Bachelor of Science in Information Technology | Bachelor of Science in Life Sciences | Bachelor of Science in Regulatory Affairs | Bachelor of Science in Statistics
Regions
Countries
States
Cities
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