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Statistical Programmer

Job in North Chicago, Lake County, Illinois, 60086, USA
Listing for: Katalyst CRO
Full Time position
Listed on 2026-10-13
Job specializations:
  • IT/Tech
    Data Scientist, Data Analyst, Information Security & Data Protection, Data Engineering
Salary/Wage Range or Industry Benchmark: 95000 - 125000 USD Yearly USD 95000.00 125000.00 YEAR
Job Description & How to Apply Below
Responsibilities
  • The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
  • The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting
  • Develop and validate SAS programs to support clinical trial data analysis and reporting
  • Create, maintain, and document SAS programming standards and procedures
  • Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met
  • Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency
  • The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry
  • Prepare datasets for analysis, including merging and cleaning data from various sources
  • Prepare and review tables, listings, and figures for clinical study reports
  • Ensure compliance with regulatory requirements and guidelines
  • Keep up to date with new SAS programming methods and software, as well as regulatory guidance
Requirements
  • Bachelor's Degree in statistics, computer science, or a similar quantitative field
  • 4+ years of clinical statistical programming experience within the pharmaceutical or related industry
  • Proficiency in SAS programming
  • Knowledge of CDISC data standards
  • Strong attention to detail and ability to work independently
  • Excellent problem-solving skills
  • Excellent verbal and written communication skills
  • Knowledge of regulatory requirements for clinical trials and drug development
  • Ability to work in a team environment and collaborate effectively with other stakeholders
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