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Biostatistical Programming Senior Associate

Amgen
Amgen
4 years
preferred by company
10 Feb. 6, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Biostatistical Programming Senior Associate
Location: Hyderabad, India (On-site)
Job ID: R-235521
Category: Clinical Development
Posted Date: February 02, 2026
Employment Type: Full Time


About the Role

Amgen is strengthening its global Statistical Programming organization, with Amgen India (AIN), Hyderabad serving as a key hub for integrated, cross-regional delivery. The Biostatistical Programming Senior Associate will play a critical role in supporting clinical studies and regulatory submissions through high-quality statistical programming and data analysis.

This position offers the opportunity to work on complex clinical trial datasets, contribute to regulatory deliverables, and collaborate with global, cross-functional teams within a leading biopharmaceutical organization.


Key Responsibilities

  • Perform statistical analysis and reporting of clinical trial data using SAS and/or R.

  • Create, validate, and maintain complex SDTM, ADaM, and other analysis datasets for safety and efficacy evaluations.

  • Develop and validate complex tables, listings, and figures (TLFs) to support clinical studies and submissions.

  • Prepare and review statistical programming specifications and related technical documentation.

  • Support the preparation of statistical programming deliverables for regulatory submissions.

  • Maintain tracking, validation, and quality documentation in compliance with internal and regulatory standards.

  • Collaborate with cross-functional teams to develop and validate programs for data quality checks and analysis verification.

  • Work closely with global study team members across functions and geographies.

  • Assist the Study Lead Programmer (SLP) or act as a backup SLP when required.

This role is based at Amgen India, Hyderabad.


Required Qualifications and Experience

  • Bachelor’s degree or higher in Biostatistics, Statistics, Mathematics, Computer Science, or a related quantitative or scientific discipline.

  • Minimum of 4 years of hands-on statistical programming experience within a clinical development or pharmaceutical research environment.

  • Strong understanding of the drug development lifecycle and clinical trial data structures.

  • Demonstrated ability to perform complex statistical programming and analysis tasks independently.

  • Proficiency in SAS, including in-depth knowledge of SAS/STAT procedures; working experience with R is an advantage.

  • Working knowledge of CDISC standards, including SDTM, ADaM, and Define.xml, with the ability to implement these standards effectively.

  • Experience using data quality, validation, and compliance check tools.

  • Proven ability to deliver high-quality outputs under tight timelines and manage multiple projects simultaneously.

  • Strong written and verbal communication skills in English.

  • Ability to work effectively in a globally distributed, cross-cultural team environment.


Preferred Qualifications

  • Master’s degree or higher in Statistics, Biostatistics, Mathematics, or a related quantitative discipline.

  • Experience with open-source programming tools such as R and Python, as well as automation platforms and emerging technologies in statistical programming.

  • Prior experience supporting regulatory submissions for drug approvals.


Why Join Amgen

Amgen offers a dynamic and inclusive work environment focused on innovation, collaboration, and patient impact. Employees benefit from extensive global career development opportunities, continuous learning, and a comprehensive total rewards program that supports health, financial well-being, work-life balance, and long-term career growth.


Apply now on thepharmadaily.com to advance your career in biostatistical programming with a global biotechnology leader.