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Amgen

Makes biotech medicines for serious illnesses

Biostatistical Programming Senior Associate

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-timeTaipei City, TaiwanNo salary listedIn-person

About the Job

Requirements

  • A Master's degree in Statistics, Biostatistics, or a related subject with high statistical content, plus 2 years of post-graduate experience as a statistician in the pharmaceutical industry or medical research; or a doctoral degree in those fields with 1 year of post-graduate experience.
  • Competency in statistical programming using SAS or R.
  • Experience applying statistical methods in the analysis and conduct of clinical trials.
  • Ability to communicate clearly in English, both in writing and orally.

Responsibilities

  • Author and provide statistical contributions to Statistical Analysis Plans, Table/Figure/Listing shells, randomization specifications, submission data file specifications (SDTM/ADaM), and other key study-related documentation.
  • Conduct and document statistical analyses for clinical trials, including primary and secondary endpoint analyses, exploratory analyses, and dose-level review support.
  • Perform and document quality control of datasets and outputs to ensure accuracy, consistency, and compliance with CDISC standards.
  • Participate in Clinical Study Team meetings to provide statistical input and represent Biostatistics.
  • Collaborate with programming colleagues to ensure timely delivery of study outputs.
  • Contribute to clinical publications, study reports, and regulatory submissions.
  • Support the review of deliverables from external suppliers for quality.
  • Stay current with new methodologies, tools, and regulatory guidelines in statistical practice.
  • Ensure statistical sections of the Trial Master File are maintained and up to date.
  • Adhere to company policies, standard operating procedures, and relevant controlled documents, and support audits as needed.

Desired Qualifications

  • A Master's degree with 4 or more years of post-graduate experience, or a doctorate with 2 or more years.
  • Prior leadership of at least one study or project with minimal oversight.
  • Experience authoring protocols and Statistical Analysis Plans, and reviewing Clinical Study Reports.
  • Familiarity with CDISC standards, including SDTM and ADaM.
  • Experience with artificial intelligence or automation tools to drive efficiency.
  • Strong understanding of drug development and statistical applications across the clinical lifecycle.

About the Company

Amgen

Makes biotech medicines for serious illnesses

Amgen develops and makes biologic medicines, which are drugs built from proteins and antibodies grown in living cells, for serious conditions such as heart disease, cancer, and bone loss. Its anemia drug Epogen, approved in 1989, became one of the biotechnology industry's first blockbuster medicines. Amgen grows these drugs in large tanks called bioreactors, and its products include the cholesterol drug Repatha, the bone-building drug Evenity, and the severe asthma drug Tezspire. It earns money by selling these medicines, mostly through large drug wholesalers that supply hospitals and pharmacies. Amgen was founded in 1980 and is based in Thousand Oaks, California.

Company size
10,001+
Company stage
IPO
Headquarters
Thousand Oaks, CA
Founded
1980

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