Biostatistical Programming Senior Associate
Tasks
- Analyze clinical trial data
- Create and validate analysis datasets
- Create and validate tables, listings, and figures
- Develop safety and efficacy programs
- Maintain tracking and validation documentation
- Prepare regulatory submissions documents
- Prepare statistical programming specifications
- Report clinical trial data
- Support statistical programming documentation
- Validate data quality programs
Perks/Benefits
Skills/Tech-stack
Automation | CDISC ADaM | CDISC Define | CDISC SDTM | Clinical data | Data Quality | Development Life Cycle | Drug development | Drug development life cycle | Python | R | Regulatory Submissions | SAS | SAS Stat
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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