Associate Director, Statistical Programming
Redwood City, California, United States
USD 229K-269K Mid-level Full Time
Tasks
- Build and execute SAS programs for data analysis exploratory and post hoc reviews
- Create reviewer ready outputs and reviewer guides
- Develop SAS macros and tools for repeated program use
- Develop specifications for statistical analysis plan and clinical study report
- Ensure CDISC compliance and submission readiness for study data packages
- Evaluate CDISC electronic data packages for completeness and regulatory compliance
- Maintain programming standards for validation repeated use and TMF archival
- Manage on time and quality delivery of CRO generated analysis results
- Plan execute and validate SAS statistical programming for clinical trial analyses
- Review CRO generated case report forms database and data transfer specifications
- Validate CRO generated data and analysis results
Perks/Benefits
- N/A
Skills/Tech-stack
ADaM | CDISC | Clinical Trial Data | Clinical trial | Clinical trial data standards | Data Standards | Define-XML | FDA guidance | Pinnacle 21 | Project Management | R Shiny | SAS | SAS Access | SAS Graph | SAS Macro | SAS Stat | SDTM | Spotfire | Tableau
Education
Regions
Countries
States
Cities
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