Associate Clinical SAS Programmer/Junior Statistician (SAS)

Location: San Francisco Bay Area, California; hybrid. Compensation also includes a range of $71,000–$92,000 for other locations.

Salary: $86,000–$112,000 yearly base compensation for the San Francisco Bay Area, plus bonus.

Company

hirify.global is a publicly traded medical technology company developing AI-driven, non-invasive solutions for diagnosing and managing coronary artery disease.

What you will do

• Develop, validate, and maintain SAS programs that transform raw clinical data into SDTM and ADaM datasets.
• Create dataset specifications from protocols and electronic case report forms, and support Statistical Analysis Plans and TFL mock-ups.
• Program, test, and validate tables, listings, and figures for conferences, publications, clinical study reports, interim analyses, and safety monitoring.
• Perform descriptive statistics, t-tests, ANOVA, basic regression modeling, and other routine clinical trial analyses.
• Conduct independent double-programming and quality control to ensure accurate, reproducible results and compliance with CDISC standards and SOPs.
• Support clinical research teams, principal investigators, data management, statisticians, and programmers while managing timelines, protocol amendments, and urgent data requests.

Requirements

• Bachelor’s degree in a science or health-related field and 3–4 years of relevant experience.
• Advanced proficiency in Base SAS, SAS/STAT, SAS/GRAPH, SAS/Macro, and SQL.
• Hands-on experience implementing SDTM and ADaM models and familiarity with EDC systems and clinical data structures.
• Solid understanding of biostatistical methods, including survival, longitudinal, and categorical data analysis.
• Knowledge of ICH Guidelines, US FDA requirements, and European clinical trial regulations.
• Excellent written and oral English communication skills required.

Nice to have

• Experience integrating Python with SAS for clinical trial analytics.
• Experience in cardiovascular medical device clinical research.
• Experience with registry studies or investigator-initiated studies.

Culture & Benefits

• Work in a fast-paced startup environment with a smaller, collaborative team.
• Participate in process improvement and cross-functional SOP development.
• Manage multiple projects with shifting priorities and opportunities to learn new techniques.
• Work on products used in clinical care and cleared for use in the US, UK, Europe, Japan, and Canada.
• Bonus available in addition to base compensation.