Senior Statistical Programmer
Tasks
- Build SAS coding and macro libraries
- Coordinate statistical programming activities across clinical projects
- Develop algorithms and programs for datasets
- Ensure work aligns with GCP ICH and 21 CFR part 11
- Import and export data
- Independently check outputs for consistency
- Maintain CDISC guidance and FDA compliance
- Manage clinical data warehouse libraries
- Mentor less experienced statistical programmers
- Prepare clinical trial datasets for regulatory submission
- Produce data listings, summary tables, and graphs
- Support data edit checks for data cleaning
- Write specifications for analysis datasets
Perks/Benefits
- 401k employer match
- Accrued vacation
- Health/Dental/Vision
- Life AD And D Insurance
- Long-term disability
- Paid Holidays
- Paid parental leave
- Paid sick time
- Short-term disability
Skills/Tech-stack
21 CFR | 21 CFR Part 11 | ADaM | BRIDG | CDASH | CDISC | CFR Part 11 | Controlled Terminology | Data Management | Data Warehousing | Define and controlled terminology | DefineXML | Electronic submissions | GCP | ICH | Kaplan-Meier | Metadata Management | ODM | Oracle Inform | Part 11 | Rave | SAS | SAS Graph | SAS Macro | SAS SQL | SAS Stat | SAS/ODS | SDTM | SHARE
Education
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