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Amgen Logo Amgen · Research and Development

Senior Associate Biostatistical Programming

Taiwan, Taipei · Job Posted February 14, 2026
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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
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Senior Associate Biostatistical Programming

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Senior Associate Biostatistical Programming

Amgen is seeking a Senior Associate Biostatistical Programmer to join CfOR in Ta...
Location
Location
Taiwan , Taipei
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
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
Job Responsibility
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
What we offer
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
  • Fulltime
Read More
Arrow Right

Senior Associate Biostatistical Programming

Amgen is seeking a Senior Associate Biostatistical Programmer to join CfOR in Ta...
Location
Location
Taiwan , Taipei
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
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
Job Responsibility
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
What we offer
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
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Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...
Location
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Expiration Date
Until further notice
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Requirements
Requirements
  • BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects, with at least 4 years of statistical programming experience in relevant career statistical programming experience in a clinical development environment
  • Familiarity with drug development life cycle and excellent skills with the manipulation, analysis and reporting of complex clinical trial data
  • Ability to effectively perform complex statistical programming and related tasks
  • Ability to provide quality output and deliverables in adherence with challenging timelines
  • Ability to work effectively on multiple tasks or projects across therapeutic areas
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
  • Working knowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards with strong ability to implement the standards
  • In depth knowledge of SAS/STAT packages
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  • Excellent oral and written English communication skills
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Job Responsibility
  • Analysis and reporting of clinical trial data using SAS and/or R
  • Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
  • Creation and validation of complex tables, listings, and figures, both safety and efficacy
  • Prepare statistical programming specifications
  • Prepare statistical programming related documents for regulatory submissions
  • Maintain tracking and validation documentation
  • Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
  • Interact and collaborate with study team members from other functions globally
  • Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP
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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
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Biostatistical Programming Senior Associate

If you feel like you’re part of something bigger, it’s because you are. At Amgen...
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India , Hyderabad
Salary
Salary:
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Expiration Date
Until further notice
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Requirements
Requirements
  • BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects, with at least 4 years of statistical programming experience in relevant career statistical programming experience in a clinical development environment
  • Familiarity with drug development life cycle and excellent skills with the manipulation, analysis and reporting of complex clinical trial data
  • Ability to effectively perform complex statistical programming and related tasks
  • Ability to provide quality output and deliverables in adherence with challenging timelines
  • Ability to work effectively on multiple tasks or projects across therapeutic areas
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
  • Working knowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards with strong ability to implement the standards
  • In depth knowledge of SAS/STAT packages
  • Familiar with data quality and compliance check tools
  • Excellent oral and written English communication skills
Job Responsibility
Job Responsibility
  • Analysis and reporting of clinical trial data using SAS and/or R
  • Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
  • Creation and validation of complex tables, listings, and figures, both safety and efficacy
  • Prepare statistical programming specifications
  • Prepare statistical programming related documents for regulatory submissions
  • Maintain tracking and validation documentation
  • Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
  • Interact and collaborate with study team members from other functions globally
  • Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP
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Expiration Date
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Requirements
Requirements
  • 5-9 years of overall experience
  • BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or related subject
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  • Biostatistical programming using SAS version 8.2 and higher or other programming languages (e.g. R or Python)
  • Understanding of computer operating systems, including UNIX, preferred
  • Project planning and management
  • Basic understanding of IRT systems preferred
  • Drug development processes and operations
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Job Responsibility
  • Creating and delivering Participant and Investigational Product (IP) randomization lists meeting specifications per randomization requests
  • Perform the duties of a Study Randomizer as needed
  • Write and validate SAS programs to verify randomization assignments and dose decisions performed by an Interactive Response Technology (IRT) system throughout the conduct of a clinical trial
  • Function as a study programmer to manage IRT data transfer activities
  • Act as a gatekeeper for IRT data transfers into Amgen’s secure File Transfer Protocol (sFTP) locations
  • Understand and execute both department and study level macros and utilities
  • Ongoing verification of electronic systems used to execute randomization schedules and dosing algorithms
  • Ensuring procedures are followed to maintain the study blind per Amgen Study Operating Procedures (SOPs) throughout the lifecycle of a study
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Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
  • At least 4 years of statistical programming experience in a clinical development environment
  • Familiarity with drug development life cycle
  • Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
  • Ability to effectively perform complex statistical programming and related tasks
  • Ability to provide quality output and deliverables in adherence with challenging timelines
  • Ability to work effectively on multiple tasks or projects across therapeutic areas
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
  • Working knowledge of latest CDISC SDTM standards
  • Familiar with CDISC ADaM and Define standards with strong ability to implement the standards
Job Responsibility
Job Responsibility
  • Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
  • Analysis and reporting of clinical trial data using SAS and/or R
  • Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
  • Creation and validation of complex tables, listings, and figures, both safety and efficacy
  • Prepare statistical programming specifications
  • Prepare statistical programming related documents for regulatory submissions
  • Maintain tracking and validation documentation
  • Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
  • Interact and collaborate with study team members from other functions globally
  • Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP
What we offer
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
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Arrow Right

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
  • At least 4 years of statistical programming experience in a clinical development environment
  • Familiarity with drug development life cycle
  • Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
  • Ability to effectively perform complex statistical programming and related tasks
  • Ability to provide quality output and deliverables in adherence with challenging timelines
  • Ability to work effectively on multiple tasks or projects across therapeutic areas
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
  • Working knowledge of latest CDISC SDTM standards
  • Familiar with CDISC ADaM and Define standards with strong ability to implement the standards
Job Responsibility
Job Responsibility
  • Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
  • Analysis and reporting of clinical trial data using SAS and/or R
  • Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
  • Creation and validation of complex tables, listings, and figures, both safety and efficacy
  • Prepare statistical programming specifications
  • Prepare statistical programming related documents for regulatory submissions
  • Maintain tracking and validation documentation
  • Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
  • Interact and collaborate with study team members from other functions globally
  • Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP
What we offer
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
  • Fulltime
Read More
Arrow Right

Biostatistical Programming Senior Associate

Amgen is expanding its global Statistical Programming capabilities, with Amgen I...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or other related quantitative or scientific subjects
  • At least 4 years of statistical programming experience in a clinical development environment
  • Familiarity with drug development life cycle
  • Excellent skills with the manipulation, analysis and reporting of complex clinical trial data
  • Ability to effectively perform complex statistical programming and related tasks
  • Ability to provide quality output and deliverables in adherence with challenging timelines
  • Ability to work effectively on multiple tasks or projects across therapeutic areas
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
  • Working knowledge of latest CDISC SDTM standards
  • Familiar with CDISC ADaM and Define standards with strong ability to implement the standards
Job Responsibility
Job Responsibility
  • Perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions
  • Analysis and reporting of clinical trial data using SAS and/or R
  • Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy
  • Creation and validation of complex tables, listings, and figures, both safety and efficacy
  • Prepare statistical programming specifications
  • Prepare statistical programming related documents for regulatory submissions
  • Maintain tracking and validation documentation
  • Collaborate with cross-functional team and create and/or validate complex programs for checking data quality
  • Interact and collaborate with study team members from other functions globally
  • Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP
What we offer
What we offer
  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging
  • 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
Read More
Arrow Right