Biostatistical Programming Senior Associate
Tasks
- Analyze clinical trial data using SAS and R
- Collaborate on data quality checking programs
- Create validate ADaM datasets
- Create validate SDTM datasets
- Create validate analysis tables listings figures
- Implement CDISC standards
- Maintain validation tracking documentation
- Prepare regulatory submission documentation
- Prepare statistical programming specifications
Perks/Benefits
Skills/Tech-stack
ADaM | CDISC | Clinical data | Clinical data standards | DEFINE | Data Quality | Data Standards | R | SAS | SAS Stat | SDTM
Education
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