Biostatistical Programming Senior Associate
Tasks
- Analyze and report clinical trial data
- Assist or serve as backup Study Lead Programmer
- Collaborate with cross-functional teams
- Create and validate analysis datasets
- Generate and validate tables, listings, and figures
- Maintain validation documentation
- Prepare regulatory submission documents
- Prepare statistical programming specifications
Perks/Benefits
- Career development
- Health benefits
- Inclusive community
- Professional growth opportunities
- Work-life balance
Skills/Tech-stack
ADaM | Clinical Data Analysis | Clinical data | Data Analysis | Data Quality | Data Quality Checks | Data Validation | Quality checks | R | Regulatory documentation | SAS | SDTM | Statistical programming | Team Collaboration
Education
Roles
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