Sr. Principal Analyst, Statistical Programming
Tasks
- Create documentation for regulatory submissions
- Develop and validate SAS programs
- Develop programming standards and procedures
- Lead statistical programming efforts
- Manage project timelines and resources
- Manage vendor activities
- Mentor and supervise programming team
- Support clinical data analysis and reporting
Perks/Benefits
Skills/Tech-stack
21 CFR | 21 CFR Part 11 | ADaM | CDISC | CFR Part 11 | Data Systems | Data Validation | Define.xml | FDA Guidelines | Part 11 | Programming Standards | R | Relational databases | SAS Base | SAS Graph | SAS Macro | SDTM
Education
Roles
Regions
Countries
States
Cities
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