Biostatistical Programming Senior Associate
Tasks
- Analyze and report clinical trial data
- Collaborate with study teams globally
- Create and validate ADaM datasets
- Create and validate SDTM datasets
- Create and validate analysis tables listings and figures
- Implement data quality checks
- Maintain tracking and validation documentation
- Prepare regulatory submission documents
- Prepare statistical programming specifications
- Support Study Lead Programmer
Perks/Benefits
Skills/Tech-stack
ADaM | CDISC Define | CDISC standards | Data Quality | R | Regulatory Submissions | SAS | SAS_STAT | SDTM
Education
Bachelor of Arts | Bachelor of Engineering | Bachelor of Science | Master of Science
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