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Senior Manager - Global Heor Value Writing Leader

14-18 years
₹50 – ₹65 LPA
10 May 23, 2025
Job Description
Job Type: Full Time Education: MD/DO/PharmD/B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Senior Manager - Global HEOR Value Writing Leader
Location: India – Hyderabad
Work Type: On Site
Job ID: R-213740
Posted On: May 5, 2025
Category: Clinical

Estimated Salary: ₹50 – ₹65 LPA


About Amgen:
At Amgen, we are driven by a mission to serve patients living with serious illnesses. Since 1980, we have pioneered breakthroughs in biotechnology across Oncology, Inflammation, General Medicine, and Rare Disease, helping millions live healthier lives. Join a science-based, innovative culture that thrives on tackling challenges and transforming patient care.


Role Summary:
The Senior Manager - Global HEOR Value Writing Leader will oversee a team of Global HEOR Value Writers and manage the timely and high-quality development of payer- and HTA-relevant deliverables. These include Global Value Dossiers (GVDs), AMCP dossiers, HTA briefing books, scientific publications, and more. This role partners closely with the Global Head of HTA Strategy & Project Management and Global HEOR Product Leads to ensure alignment with strategic goals.


Key Responsibilities:

  • Lead and mentor a team of Global HEOR Value Writers, fostering a culture of excellence and accountability.

  • Manage development, review, and quality control of GVDs, AMCP dossiers, HTA reports, and other payer-relevant materials.

  • Ensure alignment of writing outputs with product strategy, timelines, and Amgen’s internal standards.

  • Serve as a subject matter expert on payer- and HTA-related writing.

  • Collaborate on process improvements to enhance efficiency and accelerate content delivery.

  • Contribute to recruitment, onboarding, training, and performance management within the team.

  • Ensure compliance with regulatory guidelines and Good Publication Practice.


Basic Qualifications:

  • Doctorate + 2 years’ experience in HEOR, Medical, or Regulatory writing in pharma/biotech/consulting
    OR

  • Master’s + 8–10 years’ relevant experience
    OR

  • Bachelor’s + 10–14 years’ relevant experience
    OR

  • Diploma + 14–18 years’ relevant experience

Additional Requirements:

  • 3+ years in a people management capacity

  • Proven experience leading development of GVDs, AMCP dossiers, HTA deliverables


Skills & Competencies:

  • Strong leadership, mentoring, and team management skills

  • Excellent written and oral communication tailored to diverse stakeholders

  • Expertise in global HTA processes, payer requirements, and market access strategies

  • Deep understanding of clinical, real-world, and economic evidence generation

  • Proficient with Microsoft Office and citation/reference tools (e.g., EndNote)

  • Experience leveraging AI for workflow optimization


Work Culture & Benefits:

  • Collaborative and inclusive work environment

  • Competitive total rewards aligned with industry standards

  • Career development and continuous learning opportunities

  • Support for health, well-being, and work-life balance


Equal Opportunity Employer:
Amgen values diversity and is an Equal Opportunity employer. We are committed to providing reasonable accommodations for individuals with disabilities.

To apply, visit: careers.amgen.com