Senior Statistical Programmer FSP
Tasks
- Communicate with cross functional teams for project specifications and status
- Create TLFs (Tables, Listings, Figures)
- Create and review submission documents
- Generate and validate ADaM analysis datasets
- Generate and validate SDTM datasets
- Perform QC and validation programming
- Perform SAS programming for clinical trial data
- Perform efficacy analysis
- Produce complex ad hoc reports
- Support eCRTs using clinical metadata
Perks/Benefits
Skills/Tech-stack
ADaM | Ad Hoc Reporting | Ad-Hoc | CDISC | Clinical Trial Submissions | Clinical data | Clinical data management | Clinical trial | Clinical trial reporting | Data Management | Data Validation | DefineXML | Efficacy analysis | QC | SAS | SDTM | Trial reporting
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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