Biostatistical Programming Senior Associate
Tasks
- Analyze clinical trial data
- Collaborate on data quality checks
- Create and validate ADaM datasets
- Create and validate SDTM datasets
- Create and validate analysis tables listings figures
- Implement CDISC Define standards
- Maintain tracking and validation documentation
- Prepare regulatory submission documents
- Prepare statistical programming specifications
- Serve as backup study lead programmer
- Support study lead programmer duties
Perks/Benefits
- N/A
Skills/Tech-stack
ADaM | CDISC | CDISC Define | DEFINE | Data Quality | Python | R | Regulatory Submissions | SAS | SAS Stat | SDTM
Education
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