Biostatistician/SAS Programmer (Clinical Trials)

Location: Remote - US

Estimated pay range: $99,000–$129,000 per year

Company

hirify.global is a digital healthcare company developing wearable biosensors, cloud-based data analytics, and proprietary algorithms for cardiac monitoring and clinically actionable insights.

What you will do

• Design and analyze clinical trials and observational studies with cross-functional teams.
• Develop and validate SAS programs for data manipulation, statistical analysis, and report generation.
• Create and review statistical analysis plans, study protocols, and data specifications.
• Perform quality control checks on datasets, tables, listings, and figures supporting clinical, quality, production, and regulatory activities.
• Provide statistical consultation and interpret results for cross-functional stakeholders.
• Support FDA remediation, regulatory submissions, agency responses, and related documentation.

Requirements

• Master’s or PhD in Biostatistics, Statistics, or a related field.
• At least 3 years of biostatistics or statistics experience.
• Strong proficiency in SAS, including Base, Macro, SQL, and statistical procedures.
• Experience with clinical trial data and regulatory submissions, including CDISC SDTM/ADaM standards.
• Knowledge of regression, survival analysis, and mixed-model methods.
• Strong problem-solving, communication, teamwork, project-management, and attention-to-detail skills.

Nice to have

• Experience with R or STATA.

Culture & Benefits

• Remote work arrangement for candidates in the US.
• Opportunity to contribute to cardiac health solutions and patient-focused medical technology.
• Collaboration with Clinical Research, Quality, Production, regulatory, and other cross-functional teams.
• Inclusive workplace with reasonable accommodations available during the application process.