Biostatistical Programming Senior Associate
Tasks
- Analyze clinical trial data
- Collaborate on data quality checking programs
- Create and validate ADaM datasets
- Create and validate SDTM datasets
- Create and validate tables, listings, and figures
- Maintain tracking and validation documentation
- Prepare regulatory submission documents
- Prepare statistical programming specifications
- Support study lead programmer activities
Perks/Benefits
- Career development
- Diverse and inclusive workplace
- Finance and wealth benefits
- Health benefits
- Professional growth opportunities
- Work-life balance
Skills/Tech-stack
CDISC ADaM | CDISC SDTM | Compliance | DEFINE | Data Quality | R | SAS | SAS Stat
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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