Senior Statistical Programmer FSP
Tasks
- Communicate with cross functional teams for project specifications status and issues
- Conduct efficacy analysis
- Create and review submission documents and eCRFs
- Create complex ad-hoc reports from raw data
- Develop production QC and validation programming
- Generate validate SDTM ADaM datasets analysis files
- Perform SAS data manipulation analysis reporting of clinical trial data
- Provide study lead support when needed
Perks/Benefits
Skills/Tech-stack
ADaM | CDISC | Clinical Trial Data | Clinical trial | Define-XML | Efficacy analysis | QC | SAS | SDTM | Trial data | Validation
Education
Bachelor of Engineering | Bachelor of Science | Master of Science | PhD
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