Senior Statistical Programmer FSP (SAS+R)
Tasks
- Communicate with cross functional teams for project specifications and status
- Create TLFs (Tables, Listings, Figures)
- Create and review submission documents and electronic submissions
- Generate and validate SDTM and ADaM datasets and analysis files
- Generate complex ad hoc reports from raw data
- Perform SAS data manipulation analysis reporting for clinical trial data
- Perform production QC and validation programming
- Support efficacy analysis
Perks/Benefits
Skills/Tech-stack
ADaM | Ad Hoc Reporting | Ad-Hoc | CDISC | Clinical Trial Data | Clinical trial | Data Validation | Define.xml | Efficacy analysis | QC validation | SAS | SDTM | Trial data | XML
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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