Senior Biostatistical Programming (SAS)

Location: Wilmington, Delaware, United States; hybrid setup with a minimum of 3 days per week in the office. Local candidates or candidates willing to relocate to the United States only.

Company

hirify.global is a global biopharmaceutical company developing and commercializing therapeutics in Hematology, Oncology, Inflammation, and Autoimmunity.

What you will do

• Process clinical data for statistical analysis of Phase I–III clinical trials using SAS.
• Generate CDISC-compliant analysis datasets according to statistical analysis plans.
• Implement analysis methods and produce summary tables, graphs, listings, and ad hoc analyses.
• Prepare and review TLF shells and assist statisticians with statistical analysis plans.
• Run CDISC validation programs, review validation outputs, and document error-free validation reports.
• Validate programs and results produced by other programmers while working independently across studies.

Requirements

• BA/BS degree in mathematics, statistics, computer science, or a health-related field.
• Several years of SAS/Base/Macro/GRAPH programming experience in the pharmaceutical industry.
• Strong SAS programming skills and attention to detail.
• Knowledge of regulatory guidelines, including electronic submission standards.
• Strong organizational, time-management, communication, project-coordination, and leadership skills.
• Ability to work efficiently within compressed timelines and manage multiple tasks while coordinating others.
• Ability to work from Wilmington, Delaware, at least 3 days per week, as a local candidate or after relocating.

Nice to have

• Exposure to R programming.

Culture & Benefits

• Employment within a biopharmaceutical organization focused on developing treatments for patients with unmet medical needs.
• Work alongside statistical and programming teams supporting clinical development.
• Work is conducted in compliance with company SOPs and ICH guidelines.