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Senior Associate Biostatistical Programmer

amgen

New
Senior 🇬🇧 English
SQL SAS Git

Job description

About the role

Amgen's Center for Observational Research (CfOR) in Taiwan is hiring a Senior Associate Biostatistical Programmer. The role supports generating real-world evidence (RWE) through hands-on programming, data management and reporting on real-world health care data, working with epidemiologists and cross-functional teams.

Key responsibilities

  • Develop, test, validate and run code and macros that create analysis datasets, tables, listings and figures for drug development decisions
  • Lead and develop technical programming and process improvement initiatives within CfOR
  • Collaborate with peers in clinical and epidemiology functions and represent the programming team
  • Manage programming activities, solve programming issues and ensure adherence to departmental standards, SOPs and local compliance and regulatory standards
  • Write and review programming plans and dataset specifications, and review statistical analysis plans (SAPs) and data management plans (DMPs)
  • Help develop departmental policies and controlled documents, recruit programming staff, and take part in external professional organizations, conferences and meetings

Required profile

  • Bachelor's degree and at least four years of relevant statistical programming experience, including postgraduate research experience
  • Master's degree in a related field, or equivalent combinations of education and experience as stated in the posting
  • Experience establishing analysis standards, QC/QA processes and controlled change management
  • Willingness to learn regulatory-grade analyses and submission-ready deliverables, and to work with real-world healthcare data such as MDV and DeSC
  • Ability to produce validated, traceable and reproducible outputs under SOPs and quality systems

Required skills

  • SQL, SAS and R programming
  • Git-based version control and analysis documentation
  • Foundational understanding of medical statistics (study design, hypothesis testing, confidence intervals)
  • Experience or willingness to learn RWE generation in pharma or clinical trial programming

What we offer

  • Vast opportunities to learn and move up and across the global organization
  • A generous total rewards plan covering health, finance and wealth, work/life balance and career benefits
  • An equal opportunity employer with reasonable accommodations for disabilities

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Source : ats:workday

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Published 23 hours ago

Expires 1 month from now

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