Biostatistical Programming Senior Associate
Tasks
- Analyze clinical trial data
- Collaborate globally with cross-functional teams
- Create and validate ADaM datasets
- Create and validate SDTM datasets
- Create and validate analysis datasets
- Create tables, listings, and figures
- Maintain tracking and validation documentation
- Perform data quality compliance checks
- Prepare regulatory submission documents
- Prepare statistical programming specifications
- Support Study Lead Programmer
- Validate program results for data quality
Perks/Benefits
Skills/Tech-stack
CDISC ADaM | CDISC Define | CDISC SDTM | Clinical data | Clinical data standards | Data Quality | Data Standards | Python | R | Regulatory Submissions | SAS | SAS Stat
Education
Bachelor of Engineering | Bachelor of Science | Master of Science | PhD
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