Biostatistical Programming Sr Mgr in Uxbridge

What you will do

• Provide operational and technical leadership for Real-World Evidence (RWE) biostatistical programming within the Centre for Observational Research (CfOR).
• Lead and develop programming teams, partnering closely with epidemiologists and cross‑functional stakeholders across multiple time zones to deliver high‑quality RWE from large healthcare data sources, including electronic health records (EHR) and healthcare claims databases.
• Reporting to the local Director of Biostatistical Programming, oversee project delivery, resource planning, technical excellence, and compliance with departmental standards and processes to support regulatory, publication, and enterprise objectives.
• Lead and develop programming staff, including mentoring, workload planning, and performance oversight.
• Partner with epidemiologists, RWE scientists, and programming leads to generate robust real‑world evidence from healthcare data assets.
• Provide technical leadership and guidance in statistical programming methods, standards, and best practices.
• Manage programming activities, timelines, deliverables, and resource allocation across multiple projects and priorities.
• Ensure programming activities comply with departmental standards, SOPs, quality expectations, and regulatory requirements.
• Author, review, and approve programming plans, analysis dataset specifications, macros, and other key study documentation.
• Contribute to the development, validation, and execution of analysis datasets and outputs supporting regulatory submissions, publications, and scientific communications.
• Oversee outsourced programming activities and ensure quality and delivery expectations are met.
• Lead and contribute to process improvement initiatives, capability development, and continuous improvement across CfOR and R&D.
• Support audit readiness activities and participate in internal and external audits, inspections, and quality reviews as required.
• Represent the programming function within cross‑functional teams, governance discussions, and professional forums.
• Support recruitment, onboarding, and development of programming talent within the organization.

What we expect of you

• Degree educated.
• Relevant statistical programming experience within life sciences, clinical development, or observational research.
• Experience leading people, projects, programs, or resource allocation activities within a programming environment.
• Experience working with real‑world healthcare data, including healthcare claims and EHR databases.
• Strong programming expertise in SAS and SQL.
• Knowledge of observational research methods, drug development, and epidemiology principles.
• Strong communication, collaboration, and stakeholder management skills.
• Demonstrated leadership, problem‑solving ability, innovation, and attention to detail.
• Experience with R and/or Python is preferred but not mandatory.

What you can expect of us

• Vast opportunities to learn and move up and across our global organization.
• Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act.
• Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits.

Equal Opportunity Statement

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.