Associate Principal Scientist, Statistical Programming

About the role

Support statistical programming activities for multiple late‑stage drug or vaccine clinical development projects, delivering high‑quality analysis datasets, tables, listings and figures for regulatory submissions and post‑marketing support.

Key responsibilities

• Develop and execute statistical analysis deliverables across individual trials to worldwide regulatory applications.
• Design, maintain and validate statistical datasets for clinical development, outcomes research and safety evaluation.
• 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 project life‑cycle, ensuring compliance with SOPs, global standards and good programming practices.
• Participate in departmental strategic initiatives and travel up to 10% domestically.

Required profile

• Bachelor’s (9 years) or Master’s (7 years) degree in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field.
• Minimum 7 years of experience in SAS clinical trial programming, leading complex projects, and coordinating programming teams.
• Experience with CDISC, ADaM standards and U.S./global regulatory submissions at a leadership level.
• Strong knowledge of statistical terminology, models, and database design for analysis and reporting.

Required skills

• SAS (data steps, procedures, MACRO, GRAPH)
• Clinical trial programming and data management concepts
• CDISC and ADaM standards
• Statistical programming algorithm design
• Regulatory submission deliverables development

What we offer

• Salary range $145,475 – $224,100 per year
• Annual bonus and long‑term incentive eligibility
• Comprehensive benefits: medical, dental, vision, 401(k), paid holidays, vacation, sick and compassionate days
• Full‑time telecommuting (remote work)