Statistical Programmer

Astek • Posted Sep 12, 2025

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Job Description

Program under SAS BASE/STAT/GRAPHS/MACROS according to statistical analysis plan specifications, analysis datasets, tables, listings, and graphs for multiple clinical trials including regulatory submission activities. Provide recommendations for programming specifications and statistical output specifications in consultation with statisticians. Validate SAS programs and outputs (tables, listings, figures). Provide feedback in English during meetings and activities related to statistical reporting.

Key Requirements

  • Scientific, Computer Science, or Statistics degree (Bac+2 to Bac+5, e.g., DUT STID, Professional Licenses, Masters)
  • At least 2 years of professional experience
  • Proficiency in SAS programming
  • Experience with FDA submissions is a plus
  • At least 2 years of CDISC programming experience
  • Good written and oral English skills
  • Organized, rigorous, flexible, team player with strong analytical and synthesis skills

Required Tech & Skills

SAS programmingStatistical analysisClinical trial data managementCDISC programmingRegulatory submissionTeamworkAnalytical thinking