Statistical Analyst (Hybrid)

📋 Description

• Leads the statistical programming activities for routine studies
• Create documentation for regulatory filings including reviewers guides and data definition documents
• Participate in the development of standard SAS Macros, as well as, presenting information on
• Produce dynamic and static data visualizations to communicate quantitative analyses
• Develop SAS programs for the creation of ADaM data sets following CDISC standards
• Develop SAS programs for the creation of Tables, Listings and Figures

🎯 Requirements

• MS in Statistics, Computer Science or a related field with 2+ years of relevant experience OR BS in
• Experience in pharmaceutical clinical trials
• Demonstrated practical understanding of SAS programming related to drug development
• Experience creating and reviewing ADaM datasets for analysis
• Demonstrated ability to support efficacy analyses across clinical development phases and
• Ability to communicate clearly both oral and written

🎁 Benefits

• Paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance
• 401(k)
• Short-term incentive programs