Senior Statistical Programmer

4 weeks ago


Philadelphia, Pennsylvania, United States Saxon Global Full time
Job Title: Principal Statistical Programmer

We are seeking a highly skilled Principal Statistical Programmer to join our team at Saxon Global. As a key member of our biopharmaceutical team, you will be responsible for processing clinical data required for statistical analysis of Phase I - III clinical trials, and leading project teams.

Key Responsibilities:
  • Provide quality deliverables by following corporate and departmental policies, procedures, and applicable standards
  • Perform data manipulation, analysis, and reporting of clinical trial data
  • Create analysis files, tables, listings, and figures and validation of those files
  • Maintain project tracking and validation documentation
  • Work well in an environment where team members may be distributed across multiple locations
  • Review planning documents (Statistical Analysis Plan, dataset specifications, etc.) to ensure project objective alignment, clarity, accuracy, and completeness of programming requirements
  • Present statistical programming concepts to non-programming team members as necessary
  • Collaborate effectively with cross-functional teams and interface with multiple stakeholders to manage timelines and priorities
  • Serve as back-up to Principle Statistical Programmer as needed
Required Qualifications:
  • BA/BSc or Master's in Statistics, Mathematics, Computer Science, Life Sciences, or other related scientific subject with 7-8+ years of relevant experience
  • Extensive regulatory submission and response experience
  • In-depth SAS Programming background with excellent analysis and reporting skills
  • Command of drug development life cycle and experience with the manipulation, analysis, and reporting of clinical trials data
  • Thorough knowledge of latest CDISC SDTM, ADaM, and Define standards
  • Ability to effectively oversee geographically diverse programming teams
  • Familiarity with other programming languages (e.g. Java, R, or S-Plus)
  • Project management or project planning experience on small to large scale drug development projects
  • In-depth knowledge of SAS Graph and Stat packages


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