Senior Scientist Statistical Programming (Clinical SAS)

Location: Hybrid in North Wales, Pennsylvania, or Rahway, New Jersey, United States; US, Canada, and Puerto Rico residents only. Domestic relocation is listed as available, with 10% travel.

Salary: $117,000–$184,200 annually for the primary location; annual bonus and long-term incentive may also apply.

Company

hirify.global’s BARDS organization supports drug and vaccine discovery, development, regulatory approval, manufacturing, and marketing through quantitative science.

What you will do

• Develop and validate statistical analysis and reporting deliverables, including safety and efficacy datasets, tables, listings, and figures.
• Design and maintain statistical datasets supporting clinical development, outcomes research, and safety evaluation.
• Serve as the statistical programming point of contact across the product lifecycle.
• Maintain project plans, forecast resources, and coordinate global programming teams including outsourced staff.
• Contribute to departmental strategic initiatives and ensure timely, high-quality project delivery.

Requirements

• BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering, or a related field plus at least 5 years of SAS programming experience in a clinical trial environment; or an MS in one of these fields plus at least 3 years of such experience.
• Significant expertise in SAS clinical trial programming, including data steps, procedures, SAS/MACRO, SAS/GRAPH, systems, and databases.
• Experience developing analysis and reporting deliverables for R&D projects, including data, analyses, tables, graphics, and listings.
• Experience with CDISC and ADaM standards, clinical data management concepts, process compliance, and deliverable quality.
• Ability to design complex programming algorithms, understand analysis plans and statistical terminology, and anticipate stakeholder requirements.
• Project-level leadership, independent execution, effective negotiation, collaboration, written, oral, and presentation skills.
• Ability to turn strategy into tactical activities and design statistical databases that optimize analysis and reporting.

Nice to have

• Experience with GenAI tools, R, R Shiny, R Force, Python, or Claude.
• Drug or vaccine regulatory submission experience, including electronic submission deliverables.
• Experience directing or mentoring programmers and ensuring consistency across protocols and projects.
• Experience working across cultures and geographies and with global outsource programming staff.
• Experience managing project plans with Microsoft Project or a similar tool, professional society activity, and process improvement experience.

Culture & Benefits

• Hybrid work arrangement with comprehensive medical, dental, vision, insurance, retirement, 401(k), paid holidays, vacation, compassionate, and sick days.
• Inclusive environment focused on diverse perspectives, respectful challenge, and collaborative problem-solving.
• Regular employee status with visa sponsorship available.