IQVIA

Senior Statistical Programmer

IQVIA

full-time

Posted on:

Origin:  • 🇺🇸 United States

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Job Level

Senior

About the role

  • Utilize SAS to develop clinical study report materials for regulatory submissions
  • Import data from various sources
  • Program quality control checks for source data and reporting data issues
  • Interpret project level requirements and develop programming specifications
  • Write programming code following Good Programming Practices
  • Program SDTM and ADaM datasets and create statistical analysis tables, listings and figures
  • Validate datasets and statistical outputs per prescribed gate checks
  • Communicate with internal and client statisticians and clinical team members
  • Use and promote established standards, SOPs, and methodologies
  • Export data and clinical study report materials
  • Provide training and mentoring to team members and department staff

Requirements

  • Master’s or Bachelor’s degree in Biostatistics, Statistics, Mathematics, or Computer Science
  • Strong educational or practical evidence in programming
  • 5+ experience in Statistical Programmer role from CRO/Pharma with ADaM/SDTM/ TLFs
  • Experience in programming in SAS within the CRO/Pharma/Biotech/Healthcare industries
  • Knowledge of statistics and routine and occasionally complex analytical skills
  • Focus on quality, accuracy, and completeness of work
  • Excellent communication skills
  • Good understanding of Good Clinical Practice and ICH guidelines
  • Ability to independently lead and estimate programming scope of work
  • Take initiative and work with integrity
  • Ability to establish and maintain effective working relationships