Senior Statistical Programmer (Medtech)

Location: Remote within the contiguous United States; travel 10–20%.

Salary: USD 100,000–115,000 annually.

Company

hirify.global is a commercial-stage medtech company developing the Edison® System, a non-invasive histotripsy therapy for liver tumors and future applications across multiple disease areas.

What you will do

• Contribute to statistical analysis plans and propose analysis approaches with the clinical data scientist.
• Define, develop, validate, and execute specifications, shells, analysis datasets, tables, listings, and figures for clinical trials, real-world evidence, and observational studies.
• Write, maintain, review, and troubleshoot primarily SAS programs, including complex and non-standard outputs.
• Lead quality control and validation, including independent or double programming and review of other programmers’ work.
• Interpret analysis outputs and incorporate tables, listings, and figures into clinical study reports and other downstream deliverables.
• Maintain traceability, reproducibility, data standards, documentation, reusable code, and macros while partnering with Data Management, Regulatory Affairs, and Quality Assurance.

Requirements

• Bachelor’s or Master’s degree in statistics, computer science, mathematics, data science, epidemiology, or a related technical field, plus at least 5 years of statistical programming experience in clinical research.
• Advanced statistical programming proficiency in SAS or R; SAS is preferred, including complex analysis datasets and tables, listings, and figures.
• Familiarity with CDISC standards, including SDTM and ADaM.
• Working knowledge of statistical methods used in clinical trials and the ability to contribute to analysis planning and interpret outputs.
• Strong understanding of tables, listings, figures, and clinical study data.
• Ability to work independently, manage multiple deliverables and deadlines, and collaborate cross-functionally.
• Strong attention to detail, a quality-control mindset, and ability to review others’ work.
• Good written and verbal communication skills.

Nice to have

• Experience producing tables, listings, and figures for clinical study reports or regulatory submissions.
• Familiarity with FDA and global regulatory guidelines and standards, including ISO 14155 and ICH.
• Experience in medical device or pharmaceutical clinical trials.
• Familiarity with Tableau, Spotfire, R Shiny, or Python Dash.

Culture & Benefits

• Full-time employment with health, dental, and vision insurance.
• Life, short-term disability, and long-term disability insurance.
• 401(k), paid time off, and additional benefits.
• Work in a cross-functional medtech environment combining clinical science and real-world application.