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Biostatistics Sr Associate – Data Visualization

Amgen
India - Hyderabad
On-site

About this role

Job title: Biostatistics Sr Associate – Data Visualization

About the Role Amgen is expanding its global Biostatistics capabilities, with Amgen India playing a key role in integrated delivery and functional leadership. As a Biostatistics Senior Associate, you will provide hands-on statistical expertise to clinical studies across the drug development lifecycle. You will author and review statistical documents, perform data analyses, and collaborate cross-functionally to ensure scientific rigor, regulatory compliance, and timely delivery of study outputs. This role provides an opportunity to gain breadth across statistical deliverables while developing depth in clinical trial methodology, programming, and cross-functional teamwork.

What You'll Do

  • Apply biostatistical methods to analyze and interpret clinical trial data
  • Develop and maintain statistical programming solutions using R for data analysis, reporting, and automation
  • Collaborate with cross-functional teams to ensure timely delivery of study outputs
  • Support study teams with regulatory submission deliverables following industry standards such as CDISC (SDTM, ADaM) where applicable
  • Stay abreast of new methodologies, tools, and regulatory guidelines in statistical practice
  • Build automated workflows and reproducible reporting pipelines to improve efficiency and quality of statistical outputs
  • Contribute to process improvements and innovative technologies that optimize statistical programming and reporting workflows
  • Ensure compliance with regulatory requirements and internal quality standards
  • Assist in reviewing Amgen policies, SOPs, and controlled documents to ensure compliance
  • This position is currently located at Amgen India (Hyderabad).

What We're Looking For

  • A strategic Biostatistics leader with a passion for tech-enabled transformation
  • Master’s degree in Statistics/Biostatistics (or related subject with high statistical content) with 4 years post-graduate experience as a statistician in the pharmaceutical industry or medical research, OR Doctoral degree in Statistics/Biostatistics (or related subject with high statistical content)
  • Experience applying biostatistical methods to clinical trial data and collaborating with cross-functional teams
  • Proficiency in R and familiarity with CDISC SDTM/ADaM standards

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