Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Sr Associate Biostatistics

Amgen
Amgen
1-2 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
Location: Hyderabad, India (On-site)
Job ID: R-236392
Category: Clinical Development
Posted Date: February 02, 2026
Employment Type: Full Time


About the Role

Amgen continues to expand its global Biostatistics organization, with Amgen India (AIN), Hyderabad, serving as a strategic center for integrated delivery and functional leadership. The Senior Associate – Biostatistics will provide hands-on statistical support to clinical studies across the drug development lifecycle, ensuring high scientific quality, regulatory compliance, and timely study execution.

This position offers broad exposure to clinical trial statistics while enabling deeper expertise in statistical methodologies, cross-functional collaboration, and technology-enabled innovation within a global biopharmaceutical environment.


Key Responsibilities

  • Author and contribute to core statistical documents, including Statistical Analysis Plans (SAPs), Table/Figure/Listing (TFL) shells, randomization specifications, and SDTM/ADaM submission datasets.

  • 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 expertise and representing the Biostatistics function.

  • Collaborate closely with statistical programming teams to support timely and high-quality study deliverables.

  • Contribute to clinical study reports (CSRs), regulatory submissions, and scientific publications.

  • Review statistical deliverables from external vendors to ensure quality and compliance.

  • Maintain statistical documentation within the Trial Master File (TMF) in accordance with regulatory requirements.

  • Stay current with evolving statistical methodologies, regulatory guidelines, and emerging analytical tools.

  • Adhere to Amgen SOPs, policies, and controlled documents, and support audits and inspections as required.


Required Qualifications and Experience

  • Master’s degree in Statistics, Biostatistics, or a related discipline with high statistical content and a minimum of 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 at least 1 year of relevant post-graduate experience.

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

  • Practical 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 post-graduate 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 and quality.

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


Why Join Amgen

Amgen offers a collaborative and inclusive work environment focused on innovation, continuous learning, and patient impact. Employees benefit from global career development opportunities, a culture of belonging, and a comprehensive total rewards program covering health, financial well-being, work-life balance, and long-term career growth.