Biostatistical Programming Associate
Tasks
- Analyze and report clinical trial data using SAS and R
- Collaborate on data quality program creation and validation
- Create and validate ADaM datasets
- Create and validate SDTM datasets
- Create and validate tables, listings, and figures
- Maintain tracking and validation documentation
- Run data quality checks for safety and efficacy
- Support regulatory submissions
Perks/Benefits
- Career development
- Diversity and inclusion
- Financial benefits
- Health benefits
- Wealth benefits
- Well-being benefits
- Work-life balance
Skills/Tech-stack
CDISC ADaM | CDISC Define | CDISC SDTM | Clinical Trial Data | Clinical trial | Data Quality | Data Validation | R | SAS | SAS Stat | Statistical programming | Trial data
Education
Bachelor of Arts | Bachelor of Engineering | Bachelor of Science | Master of Science
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