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Sr Associate Biostatistics (Study Statistician)

Amgen
Amgen
2-4+ 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

Senior Associate Biostatistics (Study Statistician)
Location: Hyderabad, India (On-site)
Job ID: R-233541
Category: Clinical
Posted Date: January 13, 2026
Employment Type: Full Time


About the Role

Amgen is strengthening its global Biostatistics function, with Amgen India (AIN), Hyderabad, serving as a critical hub for integrated delivery and functional excellence. The Senior Associate Biostatistics (Study Statistician) will play a key role in supporting clinical studies across the drug development lifecycle by providing hands-on statistical expertise, ensuring scientific rigor, regulatory compliance, and timely delivery of high-quality outputs.

This role offers strong exposure to end-to-end clinical trial statistics, enabling professional growth across statistical methodologies, programming collaboration, and cross-functional teamwork within a global biopharmaceutical environment.


Key Responsibilities

  • Author and contribute to core statistical documents including Statistical Analysis Plans (SAPs), TFL shells, randomization specifications, SDTM/ADaM specifications, and other study-related documentation.

  • Perform and document statistical analyses for clinical trials, including primary, secondary, exploratory, and dose-level analyses.

  • Conduct quality control (QC) reviews of datasets and statistical outputs to ensure accuracy, consistency, and compliance with CDISC standards.

  • Participate in Clinical Study Team (CST) meetings, providing statistical input and representing the Biostatistics function.

  • Collaborate closely with statistical programmers to ensure timely and high-quality delivery of study outputs.

  • Support the development of clinical study reports (CSRs), regulatory submissions, and scientific publications.

  • Review statistical deliverables from external vendors for quality and compliance.

  • Maintain accurate and up-to-date statistical documentation within the Trial Master File (TMF).

  • Stay current with evolving statistical methodologies, regulatory guidance, and technology-enabled innovations.

  • Adhere to company SOPs, policies, and regulatory requirements, and support inspections or audits as needed.


Required Qualifications and Experience

  • Master’s degree in Statistics, Biostatistics, or a related discipline with high statistical content and 2+ years of post-graduate experience as a statistician in the pharmaceutical industry or medical research, or

  • Doctoral degree in Statistics, Biostatistics, or a related discipline with high statistical content and 1+ year of post-graduate experience.

  • Proficiency in statistical programming using SAS and/or R.

  • Hands-on experience applying statistical methods in the design, analysis, and interpretation of clinical trials.

  • Strong written and verbal communication skills in English.


Preferred Skills and Experience

  • Master’s degree with 4+ years of experience, or Doctorate with 2+ years of experience in clinical biostatistics.

  • Experience independently supporting at least one clinical study or project with minimal supervision.

  • Prior experience authoring SAPs, contributing to protocols, and reviewing CSRs.

  • Working knowledge of CDISC standards (SDTM, ADaM).

  • Exposure to AI, automation, or advanced analytics tools to improve efficiency.

  • Strong understanding of drug development processes and statistical applications across the clinical lifecycle.


Why Join Amgen

Amgen offers a collaborative, inclusive, and growth-oriented work environment where professionals can make a meaningful impact on patients worldwide. Team members benefit from continuous learning opportunities, global exposure, and a comprehensive rewards program supporting health, financial well-being, work-life balance, and long-term career development.