Sr. Scientist - Analysis and Reporting Standards, Innovation; Hybrid

In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within the company's renowned Research and Development division, quantitative scientists work alongside subject matter experts to apply scientific methodologies and tools that enable the discovery, development, regulatory approval, manufacturing and marketing of medical drugs and vaccines for the benefit of patients and global human health.

This position supports the design, development, and delivery of efficient, flexible, and modular analysis and reporting and submission standards and tools that can be used for drug and/or vaccine projects across all therapeutic areas. It adheres to standard operating procedures and departmental guidelines, drives data structures—including analysis and reporting data standards and submission standards—and actively contributes to the department’s strategic initiatives.

• Develop and validate global programming standards for ADaM datasets
• Develop and validate global programming standards for efficacy analysis and reporting
• Develop and validate global programming standards for safety analysis and reporting
• Design and develop complex programming algorithms
• Provide technical consultation and analytical support to statistical programmers and statisticians

• BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or a related field plus 5 years of statistical programming experience in a clinical trial environment
• MS in a related field plus 3 years of statistical programming experience in a clinical trial environment

• Excellent interpersonal, written, oral, and presentation skills
• Experience developing analysis and reporting deliverables for R&D projects (data, analyses, tables, listings, figures)
• Project leadership ability and independent task completion at a project level
• Expertise in clinical trial programming, including data manipulation, reporting workflows, visualization, and production‑quality practices using multiple programming languages and tools
• Knowledge of CDISC SDTM and ADaM standards
• Experience with analytical research databases and related procedures
• Understanding of statistics, clinical trial, and data management concepts as applied to drug/vaccine development

• Experience developing multilingual products for analysis and reporting using R, Python, SAS
• Experience using AI/GenAI tools such as Claude Code to enhance coding and workflow efficiency
• Ability to comprehend analysis plans and implement statistical methods not available through commercial software
• Interest in working across cultures and geographies
• Active participation in professional societies

$ – $. The salary within this range is determined by education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The employee is eligible for an annual bonus and long‑term incentive, if applicable. A comprehensive package of benefits is offered, including medical, dental, vision, and other healthcare benefits, as well as retirement benefits such as 401(k), paid holidays, vacation, and compassionate and sick days.

We are an Equal Employment Opportunity Employer. We provide equal opportunities and prohibit discrimination based on race, color, age, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability. For more information about personal rights under U.S. Equal Opportunity laws, see the EEOC resources.