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Amgen

Global HEOR Value Writing Manager

India - Hyderabad

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hirly's read of this role

Seniority
Lead / management
Country
IN
Work mode
On-site / unstated
First seen by hirly
28 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Career Category

Health Economics

Job Description

Global HEOR Value Writing Manager

Department: Global Health Economics & Outcomes Research (HEOR)

Job Family: Health Economics

Job Type: Full-Time

Location: Hyderabad, India

Reports To: Global Value Writing Team Lead

Position Summary

The Global HEOR Value Writing Manager plays a critical role in supporting Amgen’s global market access strategy through high-quality Health Technology Assessment (HTA) deliverables. This role collaborates closely with Global HEOR Product Leads to ensure alignment with product strategy. The Value Writing Manager develops Global Value Dossiers (GVDs), US AMCP dossiers, EU JCA dossiers, early HTA briefing books, reports and scientific publications ensuring content is scientifically rigorous, and will resonate with HTA and payer audiences.

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 and scientifically accurate content tailored to HTA/payer needs using evidence from clinical, economic, and real-world studies.

Contribute to HEOR publication execution, including but not limited to development of abstracts, posters, and manuscripts.

Assist in the development of training materials and onboarding documents for HEOR writing resources.

Adhere to internal processes and ensure compliance with publication and HTA standards.

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

Qualifications

Education

Bachelor’s or Master’s degree in pharmacy, health economics, medicine, public health, life sciences or a related field.

Experience

Years of relevant experience in HEOR, Medical or Regulatory writing in the pharmaceutical, biotech or consulting setting: +6 years for Master’s degree and +8 years for Bachelor’s degree.

Demonstrated experience developing value dossiers (GVDs/US AMCP) and supporting HTA submissions.

Experience in synthesizing clinical, economic, and real-world evidence into payer-relevant narratives.

Familiarity with systematic literature reviews and evidence synthesis processes.

Skills & Competencies

Excellent English oral and written communication, with ability to tailor content to different stakeholders.

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

Strong project management and organizational skills with the ability to manage multiple priorities and deadlines.

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

Knowledge of Good Publication Practice and publication submission process

Innovative use of artificial intelligence to boost efficiency.

Organizational Behaviors

Strong interpersonal and cross-functional collaboration skills.

Proactive, detail-oriented, and solutions-focused.

Comfortable working in a global team across time zones and cultures.

People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEOR teams across various time zones

.

Original posting on Amgen's site ↗

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