Senior Scientist, Statistical Programming – Late‑Stage Oncology (Hybrid)

About the role

The Senior Scientist will lead statistical programming for late‑stage oncology clinical trials, delivering analysis datasets, tables, listings and figures for regulatory submissions and post‑marketing support.

Key responsibilities

• Develop and validate analysis and reporting deliverables following global standards and SOPs.
• Coordinate a global programming team, including outsourced staff, and manage project plans with resource forecasting.
• Serve as the statistical programming point of contact throughout the product lifecycle.

Required profile

• 5+ years of SAS programming experience in a clinical trial environment (or 3+ years with an MS degree).
• Strong interpersonal, written and presentation skills with ability to collaborate across functions.
• Experience with CDISC ADaM standards and regulatory submission deliverables.

Required skills

• SAS programming (data steps, procedures, macros, SAS/GRAPH).
• CDISC ADaM and data modeling.
• Project management tools such as Microsoft Project.

What we offer

• Salary range $117,000 – $184,200 per year.
• Annual bonus, long‑term incentives, and comprehensive benefits including medical, dental, vision, 401(k) and paid time off.