Amgen Technology Private Limited

HEOR Value Writing Manager

Amgen Technology Private Limited
Hyderabad
Not disclosed
Work from OfficeWork from Office
Full TimeFull Time
Min. 6 yearsMin. 6 years

Job Description

Global HEOR Value Writing Manager

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
.

Experience Level

Mid Level

Job role

Work location
Work locationIndia - Hyderabad
Department
DepartmentHealthcare / Doctor / Hospital Staff
Role / Category
Role / CategoryPharma & Biotech Research
Employment type
Employment typeFull Time
Shift
ShiftDay Shift

Job requirements

Experience
ExperienceMin. 6 years

About company

Name
NameAmgen Technology Private Limited
Job posted by Amgen Technology Private Limited

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