Senior Manager - Global HEOR Value Writing Leader

What you will do

In this vital role you will serve as the operational head for a team of Global HEOR Value Writers (L5) supporting Amgens global market access and reimbursement.

This role is accountable for ensuring the timely and high-quality development of payer- and HTA-relevant deliverables including Global Value Dossiers (GVDs), AMCP dossiers, early HTA briefing books, reports and scientific publications across multiple therapeutic areas.

The Global HEOR Value Writing Leader aligns closely with the Global Head HTA Strategy & Project Management and the Global HEOR Product Leads on plans and timelines for the relevant deliverables.

• Lead, handle, and mentor a team of Global HEOR Value Writers, fostering a high-performance culture.
• Lead all aspects of development, review, and quality control of value writing deliverables including GVDs, AMCP dossiers, early HTA briefing materials, reports and scientific publications across multiple pipeline and inline products.
• Align with Head HTA Strategy & Project Management to ensure deliverables follow product strategy and deliverable timelines. Align with the relevant Amgen processes.
• Serve as an expert on payer- and HTA-relevant writing materials.
• Collaborate with Head HTA Strategy & Project management to implement process improvements to speed up delivery of payer- and HTA-relevant materials.
• Contribute to hiring, training, and performance evaluations within the team.
• Ensure compliance with all regulatory and quality policies and standards.

Basic Qualifications & Experience:

• Doctorate degree in health economics, public health, pharmacy, life sciences, biostatistics or a related field and 2 years of experience in HEOR, Medical or Regulatory writing in the pharmaceutical, biotech, or consulting setting OR,
• Masters degree in health economics, public health, pharmacy, life sciences, biostatistics or a related field and 8 to 10 years of experience in HEOR, Medical or Regulatory writing in the pharmaceutical, biotech, or consulting setting OR,
• Bachelors degree in health economics, public health, pharmacy, life sciences, biostatistics or a related field and 10 to 14 years of experience in HEOR, Medical or Regulatory writing in the pharmaceutical, biotech, or consulting setting OR,
• Diploma in health economics, public health, pharmacy, life sciences, biostatistics or a related field and 14 to 18 years of experience in HEOR, Medical or Regulatory writing in the pharmaceutical, biotech, or consulting setting
• Proven experience in leading the development of GVDs, AMCP dossiers, and other HTA-related documents.
• 3+ years of experience in team management capacity.

Skills & Competencies:

• Strong leadership and team management abilities.
• Excellent English oral and written communication, with ability to tailor content to different key partners.
• Advanced understanding of clinical, economic, and real-world data and their application in market access.
• Expertise in global HTA processes, payer evidence requirements, and value demonstration standard methodologies.
• Knowledge of Good Publication Practice and publication submission process
• Proficiency in Microsoft Office and reference management tools (e.g., EndNote).
• Innovative use of artificial intelligence to boost efficiency.

Organizational Behaviors:

• Proactive, collaborative, and solutions-focused leadership style.
• Strong project management and decision-making capabilities in a dynamic, distributed team environment.
• Comfortable working in a distributed team across time zones and cultures.