Statistical Programmer

📋 Description

• Analysis and reporting of clinical trial data under the direction and oversight of a Senior
• Create documentation for regulatory filings including reviewers guides and data definition documents
• Participate in the development of standard SAS Macros
• Consolidate heterogeneous data sources (e.g., clinical study databases, external databases
• Perform exploratory data analyses and visualizations in interaction with the clinical
• Produce dynamic and static data visualizations to communicate quantitative analyses

🎯 Requirements

• MS in Statistics, Computer Science or a related field with 0+ years of relevant experience OR BS in
• Demonstrated practical understanding of SAS programming or NONMEM concepts and techniques
• Ability to communicate clearly both oral and written

🎁 Benefits

• Comprehensive package of benefits including paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance and 401(k) to eligible employees
• Eligible to participate in short-term incentive programs