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Heartflow

Associate Clinical SAS Programmer/Junior Statistician

San Francisco Bay Area, California$86k–$112kentryAdded 3 days ago

About this role

HeartFlow seeks an Associate Clinical SAS Programmer/Junior Statistician to support the clinical trial lifecycle by converting raw trial data into analysis-ready datasets and generating regulatory, publication, and conference reports. You'll apply SAS programming expertise to create SDTM and ADaM datasets, perform statistical analyses, and ensure compliance with CDISC standards and FDA regulations in a fast-paced medical device environment.

What you'll do

  • Develop, validate, and maintain SAS programs to create SDTM and ADaM datasets from raw clinical databases
  • Program, test, and validate Tables, Listings, and Figures (TFLs) for conferences, publications, Clinical Study Reports, and safety monitoring
  • Perform routine statistical analyses including descriptive statistics, t-tests, ANOVA, and basic regression modeling
  • Perform independent double-programming validation to ensure 100% accuracy and reproducibility of clinical trial results
  • Assist in writing statistical methods and results sections for Clinical Study Reports, abstracts, and manuscripts
  • Manage multiple project timelines, protocol amendments, and urgent data requests while coordinating with cross-functional teams

What they're looking for

  • SAS programming (base SAS, PROC SQL, PROC REPORT)
  • CDISC standards (SDTM and ADaM models)
  • Statistical analysis (descriptive statistics, t-tests, ANOVA, regression)
  • Clinical trial data management and validation
  • Knowledge of ICH Guidelines and FDA/European regulatory requirements
  • SDTM and ADaM dataset specification development
  • Attention to detail and quality assurance in data validation
  • Project management and cross-functional collaboration
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Heartflow

Heartflow develops AI-driven cardiac diagnostic software that processes medical imaging data through cloud-based algorithmic pipelines and interactive 3D visualization tools. The company is hiring software engineers to build and refine these diagnostic systems while ensuring compliance with FDA and ISO medical device standards.

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Likely interview questions

  • Describe your experience creating SDTM and ADaM datasets—what was your role in ensuring compliance with CDISC standards?
  • Walk us through a time you caught a critical data error during validation; how did you approach the investigation and resolution?