Senior Statistical Programmer FSP
Tasks
- Create and review submission documents and eCRTs
- Create tables listings and figures for clinical trials
- Execute QC and validation programming
- Generate and validate SDTM and ADaM datasets and analysis files
- Generate complex ad hoc reports from raw data
- Perform clinical trial data manipulation analysis and reporting using SAS
- Perform define xml submissions
- Support efficacy analysis
Perks/Benefits
Skills/Tech-stack
ADaM | Ad Hoc Reporting | Ad-Hoc | CDISC | Clinical Trial Data | Clinical trial | Data Validation | DefineXML | Efficacy analysis | Oncology | Quality Control | SAS | SDTM | Trial data
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
Regions
Countries
States
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