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Global Heor Value Writing Senior Associate:

3+ years
Not Disclosed
10 Nov. 18, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Job Title: Global HEOR Value Writing Senior Associate

Location: Hyderabad, India (On-Site)

Job Type: Full-Time

Department: Global Health Economics & Outcomes Research (HEOR)

Reports To: Global Value Writing Team Lead

Job ID: R-228003


Position Summary

The Global HEOR Value Writing Senior Associate plays a pivotal role in supporting Amgen’s global market access strategy by developing high-quality Health Technology Assessment (HTA) deliverables. The role collaborates closely with the team lead and Global HEOR Product Leads to ensure alignment with product strategy. Key responsibilities include creating Global Value Dossiers (GVDs), US AMCP dossiers, EU JCA dossiers, early HTA briefing books, scientific publications, and payer-relevant content that is scientifically rigorous and aligns with HTA and payer expectations.


Key Responsibilities

  • Develop and update Global Value Dossiers (GVDs), US AMCP dossiers, EU JCA dossiers, and early HTA briefing books across multiple therapeutic areas.

  • Write clear, scientifically accurate content tailored to HTA and payer audiences, incorporating evidence from clinical trials, economic models, and real-world studies.

  • Contribute to HEOR publications, including abstracts, posters, and manuscripts.

  • Assist in developing training materials and onboarding documents for HEOR writing resources.

  • Ensure adherence to internal processes and compliance with publication and HTA standards.

  • Maintain up-to-date knowledge of HTA requirements, payer trends, and value demonstration best practices.

  • Review and quality check (QC) work of peers to ensure consistency and accuracy.

  • Participate in knowledge-sharing sessions to enhance team capabilities.


Qualifications

Education:

  • Bachelor’s or Master’s degree in Pharmacy, Health Economics, Medicine, Public Health, Life Sciences, or related fields.

Experience:

  • Minimum 3 years of relevant experience with a Master’s degree or 5 years with a Bachelor’s degree.

  • Demonstrated experience in HEOR, Medical, or Regulatory writing within pharmaceutical, biotech, or consulting settings.

  • Proven experience in developing value dossiers (GVDs/US AMCP) and supporting HTA submissions.

  • Experience synthesizing clinical, economic, and real-world evidence into payer-focused narratives.

  • Familiarity with systematic literature reviews and evidence synthesis processes.

Skills & Competencies:

  • Excellent oral and written English communication; ability to tailor content for diverse stakeholders.

  • Proficiency in Microsoft Office Suite (Word, PowerPoint, Excel); experience with reference management software (e.g., EndNote).

  • Strong project management and organizational skills, able to manage multiple priorities and deadlines.

  • Familiarity with HTA processes, global reimbursement landscapes, and payer evidence requirements.

  • Knowledge of Good Publication Practice (GPP) and publication submission processes.

  • Innovative use of artificial intelligence to improve efficiency.


Organizational Behaviors

  • Strong interpersonal skills and cross-functional collaboration.

  • Proactive, detail-oriented, and solutions-focused approach.

  • Comfortable working in a global, multi-timezone team across diverse cultures.