Senior Statistical Analyst - Programming - Oncology (Hybrid)

Added
13 days ago
Type
Full time
Salary
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Related skills

r sas regulatory filings clinical trials cdisc

πŸ“‹ Description

  • Leads the statistical programming activities for projects with lower complexity
  • Develop SAS programs for the creation of ADaM data sets following CDISC standards
  • Develop SAS programs for the creation of Tables, Listings and Figures
  • Validation of ADaM data sets, Tables, Listings and Figures
  • Create specifications for the structure of ADaM data sets for individual studies and integrated data
  • Create documentation for regulatory filings including reviewers guides and data definition documents

🎯 Requirements

  • Bachelors in Statistics, Computer Science or a related field
  • 8+ years of relevant experience in quantitative analysis (or 6+ with a Masters)
  • Experience with SAS Programming
  • Experience leading programming for clinical trials
  • In-depth understanding of SAS programming concepts and techniques related to drug development
  • Fundamental understanding of CDISC Standards

🎁 Benefits

  • Paid time off (vacation, holidays, sick)
  • Medical/dental/vision insurance
  • 401(k) to eligible employees
  • Eligible to participate in short-term incentive programs
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