Epidemiology Analyst – Real World Data & Observational Research
Location: Hyderabad, India
Company: Amgen
Job ID: R-236957
Work Type: On-Site
Category: Research / Epidemiology / Real World Evidence (RWE)
Experience Required: 8–13 Years
Education: Master’s Degree (Mandatory) | MBBS, PhD in Epidemiology or Related Field Preferred
About the Company
Amgen is a global biotechnology pioneer focused on addressing high unmet medical needs through science-driven innovation. Since 1980, the organization has advanced therapies across Oncology, Inflammation, Rare Disease, and General Medicine, delivering impactful treatments to millions of patients worldwide.
Role Overview
The Epidemiology Analyst will join the Center for Observational Research (CfOR) within the Data and Analytics Center (DAC) to support global real-world evidence (RWE) initiatives. This role contributes to observational research activities across the product lifecycle, including drug development, regulatory submissions, commercialization strategies, pharmacovigilance, and market access support.
The position is suited for experienced RWD researchers with strong methodological expertise in observational study design, epidemiologic analysis, and medical coding systems.
Key Responsibilities
Observational Research & Real-World Evidence Generation
Contribute to global observational research studies supporting drug development, registration, and commercialization.
Execute and manage descriptive epidemiologic studies assessing disease incidence and prevalence across US, EU, Asia, and emerging markets.
Conduct research using administrative claims data, electronic medical records (EMR), registries, and prospective observational cohorts.
Support pharmacovigilance studies and development of risk management plans across product lifecycles.
Data & Analytics Execution
Implement and conduct studies using real-world databases and analytics platforms such as ATLAS, Aetion, and other RWD tools.
Analyze medical claims, EHR datasets, and secondary data systems to generate regulatory and payer-relevant insights.
Partner cross-functionally to ensure methodological rigor and reproducibility.
Medical Coding & Data Integrity
Develop, review, and maintain high-quality medical codelists for exposures, outcomes, covariates, and safety endpoints.
Apply standard coding systems including ICD, MedDRA, SNOMED, and RxNorm.
Ensure regulatory readiness, clinical validity, and transparency of coding frameworks.
Scientific Communication & Publication
Conduct literature reviews and prepare research reports, manuscripts, and abstracts for peer-reviewed journals and scientific congresses.
Present complex scientific findings to internal and external stakeholders.
Serve as first or contributing author on research publications.
Methodological Excellence & Collaboration
Promote awareness and application of advanced observational research methodologies.
Stay updated with global regulatory expectations for RWE and post-marketing research.
Collaborate with multidisciplinary global teams across therapeutic areas.
Required Experience
Master’s Degree with 8–13 years of relevant experience in Epidemiology, Real World Evidence, or Observational Research.
Proven experience in pharmaceutical, biotechnology, healthcare research, or public health settings.
Hands-on experience in study design, execution, and analysis of observational research.
Experience working with secondary healthcare datasets including claims and EMR databases.
Preferred Qualifications
MBBS (or equivalent) and/or PhD in Epidemiology or related discipline with strong observational research focus.
Advanced expertise in medical coding systems such as ICD, MedDRA, SNOMED, and RxNorm.
Experience supporting regulatory submissions and drug development programs.
Demonstrated project management skills in multi-regional research initiatives.
Strong scientific writing and communication capabilities.
Core Competencies
Strong analytical and statistical reasoning
High attention to methodological rigor and data quality
Ability to manage multiple research projects simultaneously
Strong collaboration skills in global, cross-functional teams
Effective communication of complex epidemiologic findings
Why This Role Matters
This position directly supports evidence generation for regulatory authorities, payers, and healthcare stakeholders. Professionals seeking careers in Real World Evidence, Pharmacoepidemiology, Post-Marketing Research, and Global Drug Development will find significant strategic exposure and long-term growth potential in this role.
Equal Opportunity Statement
Amgen is an Equal Opportunity Employer committed to fostering a diverse and inclusive workplace. All qualified applicants will be considered in accordance with applicable employment laws.
SEO Keywords:
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