CrawlJobs Logo

Senior Associate Biostatistical Programming

amgen.com Logo

Amgen

Location Icon

Location:
Taiwan , Taipei

Category Icon
Category:
-

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided
Save Job
Save Icon
Apply Position

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

Work Type:
Hybrid work
Icon
Amgen - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Senior Associate Biostatistical Programming

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
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, 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
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, 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
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, 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
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, 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, 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
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, 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
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, 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
Read More
Arrow Right
Jobs by Category
Art and Entertainment Jobs Banking Jobs Call Center Jobs Construction Jobs Consulting Jobs Customer Service Jobs Education Jobs Energy Jobs Finance Jobs Gastronomy Jobs Health and Beauty Jobs Hospitality and Tourism Jobs Human Resources Jobs Insurance Jobs IT - Administration Jobs IT - Software Development Jobs Legal Jobs Logistics Jobs Manufacturing Jobs Marketing, Digital Marketing, SEO, SEM Jobs Media Jobs Nursing Jobs Office Administration Jobs Pharmacy Jobs Physical Work Jobs Public Relations Jobs Public Sector Jobs Purchasing Jobs Quality Control Jobs Real Estate Jobs Research and Development Jobs Sales Jobs
Job Positions Jobs by Country
United States Jobs United Kingdom Jobs India Jobs Canada Jobs Australia Jobs Germany Jobs Ireland Jobs Poland Jobs
Company
Blog About Us Contact
Follow Us
Facebook
X (Twitter)
LinkedIn
Instagram
CrawlJobs Group
ITFlashcards AllDevBlogs
© 2026 CrawlJobs Ltd. All Rights Reserved
Terms & Conditions Privacy Policy