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Global Heor Value Writing Manager

Amgen
Amgen
6-8+ years
Not Disclosed
Hyderabad, India
10 April 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

Global HEOR Value Writing Manager – Hyderabad, India

Category: Health Economics & Outcomes Research (HEOR)
Location: Hyderabad, Telangana, India
Employment Type: Full-Time | On-Site
Experience Required: 6+ years (Master’s) / 8+ years (Bachelor’s)

About the Role
We are seeking a highly skilled Global HEOR Value Writing Manager to join our Hyderabad team. This role is pivotal in supporting global market access strategies through the creation of high-quality Health Technology Assessment (HTA) deliverables. The manager will collaborate closely with Global HEOR Product Leads to ensure alignment with product strategy and deliver scientifically robust value communication to HTA bodies and payers worldwide.

Key Responsibilities

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

  • Translate clinical, economic, and real-world evidence into payer-relevant narratives and HTA-aligned content.

  • Contribute to HEOR publication activities, including abstracts, posters, and manuscripts for scientific dissemination.

  • Assist in the creation of training and onboarding materials for HEOR writing teams.

  • Ensure all deliverables comply with internal publication standards and HTA requirements.

  • Monitor and incorporate global HTA trends, payer evidence requirements, and best practices in value demonstration.

  • Leverage innovative tools, including AI, to optimize content development efficiency.

Qualifications & Experience

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

  • Experience:

    • Master’s degree: Minimum 6 years in HEOR, medical writing, or regulatory writing within pharmaceutical, biotech, or consulting environments.

    • Bachelor’s degree: Minimum 8 years in relevant roles.

    • Proven experience developing value dossiers (GVDs, AMCP dossiers) and supporting HTA submissions.

    • Skilled in synthesizing clinical, economic, and real-world evidence into compelling value narratives.

    • Familiarity with systematic literature reviews, evidence synthesis, and publication practices.

Skills & Competencies

  • Exceptional written and oral English communication; able to tailor content for diverse stakeholder audiences.

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

  • Strong project management and organizational skills, capable of managing multiple priorities and deadlines.

  • In-depth understanding of HTA processes, payer evidence requirements, and global reimbursement landscapes.

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

  • Innovative and efficient use of AI tools for content creation and workflow optimization.

Organizational & Behavioral Competencies

  • Strong cross-functional collaboration and interpersonal skills.

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

  • Ability to work effectively in a global team, across multiple time zones and cultural contexts.

  • Builds and maintains productive relationships with internal stakeholders and global HEOR teams.

Why Join Us

  • Engage in high-impact HEOR projects that shape global market access strategies.

  • Collaborate with leading experts in health economics, outcomes research, and clinical evidence.

  • Opportunity to advance your career within a global biotech/pharmaceutical organization.

  • Contribute to the development of value evidence that directly influences patient access and healthcare outcomes worldwide.

Application Instructions
Candidates meeting the qualifications are encouraged to apply online with their CV. All applications will be considered based on merit and relevance.

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