Remote SAS Programmer & Junior Clinical Statistician

Heartflow; San Francisco (CA); Remote; USD 95,000 - 135,000; Full time

Job summary

Heartflow seeks an Associate Clinical SAS Programmer/Junior Statistician in the United States to transform raw clinical trial data into analysis-ready SDTM/ADaM datasets. You will develop SAS programs and collaborate with Clinical Research staff to ensure data integrity and regulatory compliance.

You will draft SAPs, generate Tables, Listings, and Figures (TFLs), and perform descriptive statistics, t-tests, ANOVA, and basic regression to support CSRs, abstracts, and publications.

Qualifications

• Experience programming in SAS and transforming raw clinical trial data into analysis-ready datasets (SDTM/ADaM).
• Ability to draft SAPs and create Tables, Listings, and Figures (TFLs) under supervision.
• Familiarity with CDISC standards and regulatory expectations (FDA/ICH).
• Strong attention to detail and data quality, with reproducible code practices.

Responsibilities

• Develop, validate, and maintain SAS programs to create SDTM and ADaM datasets from raw clinical databases.
• Create and review dataset specifications based on protocol and case report forms (eCRFs).
• Draft and implement Statistical Analysis Plans and generate TFLs for conferences, publications, and CSRs.
• Perform routine statistical analyses (descriptive statistics, t-tests, ANOVA, basic regression) using SAS.
• Ensure compliance with CDISC standards and internal SOPs.
• Perform independent double-programming for high-risk datasets and outputs.

Skills

SAS programming

SDTM/ADaM

CDISC standards

ICH/FDA knowledge

English communication

Data analysis

Attention to detail

multi-tasking

team collaboration

statistical methods

SQL

Tools

SAS

SAS/STAT

SAS/GRAPH

SAS/Macro

SQL

Microsoft Office

Job description

Heartflow seeks an Associate Clinical SAS Programmer/Junior Statistician in the United States to transform raw clinical trial data into analysis-ready SDTM/ADaM datasets. You will develop SAS programs and collaborate with Clinical Research staff to ensure data integrity and regulatory compliance.

You will draft SAPs, generate Tables, Listings, and Figures (TFLs), and perform descriptive statistics, t-tests, ANOVA, and basic regression to support CSRs, abstracts, and publications.