Biostatistical Programming Senior Associate

Amgen · Taipei, Taiwan

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Role summary

Amgen seeks a Biostatistical Programming Senior Associate in Taipei to provide statistical expertise for clinical trials across the drug development lifecycle. The role involves authoring statistical documents, conducting data analyses, ensuring regulatory compliance, and collaborating cross-functionally to support study delivery.

What they're looking for

Master's degree in Statistics/Biostatistics or related field with 2+ years pharmaceutical industry experience, or Doctorate with 1+ year
Proficiency in statistical programming (SAS or R)
Clinical trial statistical analysis and methodology experience
Fluent written and oral English communication
Preferred: 4+ years post-graduate experience with Master's or 2+ years with Doctorate
CDISC standards familiarity (SDTM, ADaM)
Prior experience leading a study or project independently

What you'll be doing

Author and contribute to Statistical Analysis Plans, randomization specifications, and data file specifications
Conduct and document statistical analyses including primary, secondary, and exploratory endpoint analyses
Perform quality control of datasets and outputs for accuracy and CDISC standard compliance
Participate in Clinical Study Team meetings to provide statistical input and support
Collaborate with programming colleagues on timely delivery of study outputs and clinical publications

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