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Global Heor Value Writing Senior Associate

3-5 years
Not Disclosed
10 Nov. 24, 2025
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

Global HEOR Value Writing Senior Associate – Amgen (On-Site, Hyderabad, India)

Category: Health Economics
Job Type: Full-Time
Work Location: On Site
Experience Required: 3–5+ Years (as per qualifications)

About the Role

Amgen is seeking a Global HEOR Value Writing Senior Associate to support its global market access and value communication strategy. This role is a key contributor within the Global Health Economics & Outcomes Research (HEOR) function. The selected candidate will support the development of scientifically accurate, payer-focused deliverables including value dossiers and Health Technology Assessment (HTA) submissions for global markets.

The position requires strong domain expertise, excellent scientific writing skills, and the ability to translate complex clinical and economic evidence into clear, impactful narratives for HTA bodies and payers.


Key Responsibilities

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

  • Create scientifically robust content using clinical trial data, economic models, and real-world evidence tailored for HTA and payer audiences.

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

  • Support creation of training materials and onboarding content for HEOR writing teams.

  • Ensure strict adherence to internal guidelines, publication standards, and global HTA requirements.

  • Monitor evolving HTA trends, payer expectations, and advancements in value demonstration.

  • Participate in peer review and quality control of HEOR documents.

  • Engage in internal knowledge-sharing sessions to support capability building.


Qualifications

Education

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

Experience Required

  • Master’s degree holders: Minimum 3+ years of experience in HEOR, medical writing, or regulatory writing within pharmaceutical, biotechnology, or healthcare consulting settings.

  • Bachelor’s degree holders: Minimum 5+ years of relevant experience.

  • Proven experience developing GVDs, US AMCP dossiers, and supporting HTA submissions.

  • Strong understanding of clinical evidence, economic models, and real-world data for payer-focused communication.

  • Prior exposure to systematic literature reviews and evidence synthesis processes.


Skills & Competencies

  • Exceptional written and verbal communication skills in English, with ability to tailor scientific content for diverse global stakeholders.

  • Proficiency in Microsoft Word, Excel, PowerPoint; familiarity with reference management tools such as EndNote.

  • Strong project management and organizational abilities to handle multiple timelines and priorities.

  • Knowledge of HTA processes, payer evidence requirements, and global reimbursement landscapes.

  • Understanding of Good Publication Practice and publication submission workflows.

  • Ability to use AI-based tools to improve content quality and operational efficiency.


Professional Behaviors

  • Strong cross-functional collaboration and interpersonal skills.

  • Proactive, detail-oriented, and solution-driven mindset.

  • Comfortable working with global teams across multiple time zones and cultural environments.


Location: Hyderabad, India
Job ID: R-228003
Work Type: On-Site