Associate Director, Statistical Programming
Tasks
- Create dataset specifications
- Design and code SAS programs
- Develop SDTM and ADaM datasets
- Perform SAS code quality control
- Prepare eCTD documents
- Produce clinical tables figures and listings
- Review data listings
- Support ad-hoc analyses
- Support integrated summary safety and efficacy datasets
- Validate SAS code and outputs
Perks/Benefits
Skills/Tech-stack
ADaM | CDISC | Clinical Trial Data | Clinical trial | ECTD | Electronic submission | FDA electronic submission | Quality Control | R | SAS | SAS Base | SAS Graph | SAS Macros | SAS Stat | SDTM | Statistical programming | Trial data
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
Regions
Countries
States
Cities
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