Associate Director, Statistical Programming
Redwood City, California, United States
USD 229K-269K Mid-level Full Time
Tasks
- Build and execute SAS programs for internal reviews and publications
- Check submission readiness of study data packages
- Develop SAS macros for repeated analyses
- Develop programming standards for validation and repeated use
- Ensure CDISC compliance for submission packages
- Execute SAS programs for statistical analyses
- Manage CRO analysis delivery timelines
- Plan statistical programming activities
- Prepare clinical study report materials
- Review CRO analysis plans and dataset specifications
- Use CDISC validation tools for compliance checks
- Validate CRO statistical analysis data and results
Perks/Benefits
- N/A
Skills/Tech-stack
Analysis Plan | CDISC ADaM | CDISC Define | CDISC SDTM | CDISC define xml | Clinical Trial Data | Clinical study | Clinical study report | Clinical trial | Define-XML | Pinnacle 21 | Project Management | R Shiny | SAS | SAS Access | SAS Graph | SAS Macro | SAS Stat | SEND | Spotfire | Statistical Analysis | Statistical Analysis Plan | Tableau | Trial data
Education
Regions
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States
Cities
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