Biostatistical Programming Senior Associate

Amgen · Taipei, Taiwan

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Role summary

Amgen seeks a Biostatistical Programming Senior Associate in Taipei to perform statistical programming for clinical trials and regulatory submissions. The role involves complex data analysis, dataset creation, and cross-functional collaboration supporting integrated delivery across regions.

What they're looking for

BA/BSc or higher in biostatistics, statistics, mathematics, computer science, or related quantitative field
At least 4 years of statistical programming experience in clinical development
Advanced SAS/STAT proficiency and working knowledge of CDISC SDTM, ADaM, and Define standards
Proficiency with clinical trial data manipulation, analysis, and reporting
Fluent English communication skills, written and oral
Experience with data quality and compliance check tools
Ability to manage multiple projects across therapeutic areas in global teams

What you'll be doing

Perform statistical programming and analysis of clinical trial data using SAS and/or R
Create and validate SDTM, ADaM, and analysis datasets for safety and efficacy assessments
Generate and validate tables, listings, and figures for clinical and regulatory reporting
Prepare statistical programming specifications and regulatory submission documentation
Support Study Lead Programmer duties and collaborate on data quality programs

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