Senior Scientist Statistical Programming, Late-Stage (Hybrid)

About the role

This position supports statistical programming activities for late‑stage drug and vaccine clinical development projects, including leadership of one or more projects. The role involves developing and executing statistical analysis and reporting deliverables across individual trials to worldwide regulatory submissions.

Key responsibilities

• Develop and validate statistical analysis datasets, tables, listings, and figures for clinical trials and regulatory applications.
• Maintain and manage project plans, forecast resources, and coordinate a global programming team, including outsource providers.
• Serve as the statistical programming point of contact throughout the product lifecycle, ensuring timely, high‑quality deliverables.

Required profile

• BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field with at least 5 years of SAS programming experience in a clinical trial environment (or MS with 3 years).
• Strong interpersonal, written, oral and presentation skills with the ability to lead projects independently.

Required skills

• SAS
• SAS/MACRO
• SAS/GRAPH
• CDISC ADaM standards
• Microsoft Project
• Python
• R

What we offer

• Salary range $117,000 – $184,200 per year.
• Eligibility for annual bonus and long‑term incentive.
• Comprehensive benefits including medical, dental, vision, 401(k), paid holidays, vacation and sick days.