SAS Clinical Trial Programmer - TXITSP Job at NavitsPartners, Mineral Wells, TX

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  • NavitsPartners
  • Mineral Wells, TX

Job Description

SAS Clinical Trial Programmer  

Position Summary:  

  • The SAS Clinical Trial Programmer supports all phases of clinical trial data analysis, from preparation to final submission, ensuring data accuracy and reliability. 

Key Responsibilities:  

  • Develop, validate, and maintain SAS programs for clinical trial analysis. 
  • Support biostatistics teams with efficient, reproducible code. 
  • Contribute to regulatory submission documentation. 

Qualifications:  

  • Bachelor’s in a technical field; Master’s preferred. 
  • Minimum of 2 years in clinical programming. 
  • Deep understanding of clinical trial methodologies and SAS programming. 

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