Global HEOR Value Writing Manager

Amgen Inc. (IR); Hyderabad; On-site; INR 3,000,000 - 6,000,000; Full time

Job summary

Amgen seeks a Global HEOR Value Writing Manager in Hyderabad to support global market access through high-quality HTA deliverables. You will develop GVDs and dossiers, and craft content across clinical, economic and real-world data to persuade payers.

You will lead publication activities, train HEOR writers, and ensure compliance with HTA standards while collaborating with global teams across time zones.

Qualifications

• Bachelor’s or Master’s degree in pharmacy, health economics, medicine, public health, life sciences or related field.
• 6+ years HEOR/medical/regulatory writing experience for Master’s degree; 8+ years for Bachelor’s degree.
• Experience developing value dossiers (GVDs/US AMCP) and supporting HTA submissions.

Responsibilities

• Develop and update Global Value Dossiers (GVDs), US AMCP, EU JCA dossiers and early HTA briefing books.
• Write clear, scientifically rigorous content tailored to HTA/payer needs using diverse evidence.
• Contribute to HEOR publications, including abstracts, posters, and manuscripts.
• Assist in creating training materials and onboarding documents for HEOR writing resources.
• Ensure compliance with internal processes and HTA standards.
• Stay current on HTA requirements, payer trends, and value demonstration best practices.

Skills

English proficiency

MS Office

EndNote

Project management

HTA knowledge

Global teamwork

Attention to detail

AI for efficiency

Education

Bachelor’s degree in related field

Master’s degree in related field

Tools

EndNote

Microsoft Office

Job description

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.

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:

• Support and maintain effective relationships with key stakeholders
• Work effectively with global HEOR teams across various time zones

Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people’s lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.

For more information, visit www.amgen.com and follow us on www.twitter.com/amgen