Principal Statistical Programmer
United States-Massachusetts-Newton, United States
R
USD 159K-207K Senior-level Full Time
Tasks
- Advise on statistical programming timelines
- Collaborate with biostatistics data management and functional teams
- Lead statistical programming on projects
- Manage statistical programming project plans
- Monitor quality timelines resource allocation and productivity
- Provide technical support to sponsors
- Support statistical programming for clinical trials
Perks/Benefits
- N/A
Skills/Tech-stack
21 CFR Part 11 | ADaM | CDISC | CDISC compliance validation | CFR Part 11 | Clinical Trial Data | Clinical Trial Data Analysis | Clinical trial | Compliance validation | Data Analysis | Data Step | Electronic submissions | FDA 21 CFR | FDA 21 CFR Part 11 | Generating TLFs | ICH GCP | Part 11 | Pinnacle 21 | R | SAS | SAS Base | SAS Macro | SAS PROC | SAS Proc Step | SAS SQL | SAS Stat | SAS data step | SDTM
Education
Regions
Countries
States
Cities
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