Senior Statistical Programmer FSP (SAS+R)
Tasks
- Analyze clinical trial data
- Create ADaM datasets
- Create Define xml
- Create SDTM datasets
- Create submission documents
- Generate ad-hoc reports from raw data
- Generate clinical trial reports
- Manipulate clinical trial data
- Perform QC validation programming
- Perform efficacy analysis
- Produce TLFs
- Produce figures
- Produce listings
- Respond to project specifications status issues
- Review submission documents
- Validate ADaM datasets
- Validate SDTM datasets
Perks/Benefits
Skills/Tech-stack
CDISC ADaM | CDISC SDTM | Clinical Trial Data | Clinical data | Clinical data standards | Clinical programming | Clinical trial | Data Standards | Data Validation | Define-XML | Efficacy analysis | QC validation | R | SAS | TLF | Trial data
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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