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Senior Associate Biostatistical Programming

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Amgen

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Location:
Taiwan , Taipei

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Category:
Research and Development

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Contract Type:
Not provided

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Salary:

Not provided
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Job Description:

Amgen is seeking a Senior Associate Biostatistical Programmer to join CfOR in Taiwan. This role supports generating RWE through hands-on programming, data management, and generating reports based upon real-world data of health care. The programmer will partner with epidemiologists and cross-functional teams to clarify requirements, resolve issues, and deliver high-quality outputs.

Job Responsibility:

  • Develop, test, validate, and execute programming code and macros that generate analysis datasets and tables, listings, and figures to support decision making in drug development
  • Lead and develop technical programming and process improvement initiatives within CfOR
  • Represent the programming team and collaborate with peers in clinical and epidemiology functions
  • Manage programming activities and provide technical solutions to programming issues
  • Ensure programming activities adhere to departmental standards and SOPs as well as local compliance and regulatory standards
  • Write and review programming plans and dataset specifications
  • Review key study-related documents including but not limited to statistical analysis plans (SAPs) and data management plans (DMPs)
  • Participate in the development of departmental policies and controlled documents
  • Participate in the recruitment of programming staff
  • Actively participate in external professional organizations, conferences, and meetings
  • Contribute to the continuous improvement of programming processes

Requirements:

  • Master’s degree in Computer Science, Statistics, Mathematics, Life Sciences, Business Analytics, or related field OR
  • Bachelor’s degree and 2 years of directly related experience OR
  • Associate’s degree and/or 4 years of directly related experience OR
  • High school diploma / GED and 6 years of directly related experience
  • At least four (4) years of relevant statistical programming experience in a clinical development or life sciences setting, including postgraduate research experience
  • Experience in SQL, and statistical programming using SAS and R
  • Track record establishing analysis standards, QC/QA processes, and controlled change management.
  • Experience or willingness to learn the process of delivering regulatory-grade analyses and submission-ready deliverables
  • Foundational understanding of medical statistics (e.g., study design, hypothesis testing, confidence intervals).
  • Real-world evidence (RWE) generation in pharmaceutical or related research industries, or statistical programming for clinical trials
  • Strong individual contributor, proficient in developing analysis datasets, identifying data anomalies, and ensuring program accuracy
  • Motivated to learn how to work with real-world healthcare data (RWD) such as MDV and DeSC
  • Experience with Git-based version control and maintaining analysis documentation.
  • Ability to produce validated, traceable, and reproducible analysis outputs under SOPs and quality systems.
What we offer:
  • 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

Additional Information:

Job Posted:
February 14, 2026

Employment Type:
Fulltime
Work Type:
Hybrid work
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