Associate Principal Scientist, Statistical Programming

Associate Principal Scientist role supporting statistical programming for clinical development and regulatory submissions of drugs and vaccines. Requires advanced SAS expertise, clinical trial programming experience, and leadership of complex projects across global teams with direct regulatory submission involvement.

Responsibilities

• Develop and execute statistical analysis deliverables including safety and efficacy datasets, tables, listings, and figures
• Design and maintain statistical datasets supporting clinical development, outcomes research, and safety evaluation
• Lead and coordinate global programming teams including outsourced providers on multiple projects
• Serve as statistical programming point of contact and knowledge holder throughout project lifecycle
• Manage project plans, resource forecasting, and ensure timely high-quality deliverables

Requirements

• Bachelor's degree in Computer Science, Statistics, Applied Mathematics, or related field plus 9 years experience; or Master's degree plus 7 years experience
• 7+ years SAS programming experience including data steps, procedures, macros, and graphics in clinical trials
• 7+ years leading large or complex statistical programming projects with team coordination
• 7+ years designing complex programming algorithms and statistical databases
• 7+ years experience with CDISC, ADaM standards, and clinical data management systems
• 7+ years U.S. and/or worldwide regulatory submission experience at leadership level
• Strong understanding of statistical terminology, models, analysis plans, and quality assurance processes

Compensation: $142,400-$224,100 base per year, plus annual bonus and long-term incentive eligibility