Senior Statistical Programmer FSP
Tasks
- Analyze clinical trial data safety and efficacy
- Create TLF outputs
- Create and review submission documents
- Develop Define xml datasets
- Develop ad-hoc reports from raw data
- Generate ADaM datasets
- Generate SDTM datasets
- Lead programming tasks when needed
- Perform QC and validation programming
- Perform SAS data manipulation
- Respond to cross functional project inquiries
- Support efficacy analysis
- Validate CDISC datasets
Perks/Benefits
Skills/Tech-stack
ADaM | Ad Hoc Reporting | Ad-Hoc | CDISC | Clinical Trial Data | Clinical trial | Data Manipulation | Define.xml | Efficacy analysis | QC | SAS | SDTM | Trial data | Validation
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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