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Amgen

Makes biotech medicines for serious illnesses

Global HEOR Value Writing Manager

Technical WritingConfirmed live in the last 24 hours
Full-timeHyderabad, Telangana, IndiaNo salary listedIn-person

About the Job

Requirements

  • A bachelor's or master's degree in pharmacy, health economics, medicine, public health, life sciences, or a related field.
  • More than six years of relevant HEOR, medical writing, or regulatory writing experience in a pharmaceutical, biotech, or consulting setting for candidates with a master's degree, or more than eight years for candidates with a bachelor's degree.
  • Demonstrated experience developing value dossiers, including Global Value Dossiers and US AMCP dossiers, and supporting HTA submissions.
  • Experience synthesizing clinical, economic, and real-world evidence into payer-relevant narratives.
  • Familiarity with systematic literature reviews and evidence synthesis processes.
  • Excellent oral and written English communication, with the ability to tailor content to different stakeholders.
  • Proficiency in Microsoft Office Suite, including Word, PowerPoint, and Excel.
  • Experience with reference management software such as EndNote.
  • Project management and organizational skills 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 processes.
  • Innovative use of artificial intelligence to improve efficiency.
  • Ability to maintain effective relationships with key stakeholders and work effectively with global HEOR teams across time zones.
  • Ability to work across time zones and cultures.

Responsibilities

  • Develop and update Global Value Dossiers, US AMCP dossiers, EU JCA dossiers, and early HTA briefing books across multiple therapeutic areas.
  • Write clear, scientifically accurate content tailored to HTA and payer needs using evidence from clinical, economic, and real-world studies.
  • Contribute to HEOR publication execution, including developing abstracts, posters, and manuscripts.
  • Assist in developing 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.
  • Collaborate with Global HEOR Product Leads to align deliverables with product strategy.

About the Company

Amgen

Makes biotech medicines for serious illnesses

Amgen develops and makes biologic medicines, which are drugs built from proteins and antibodies grown in living cells, for serious conditions such as heart disease, cancer, and bone loss. Its anemia drug Epogen, approved in 1989, became one of the biotechnology industry's first blockbuster medicines. Amgen grows these drugs in large tanks called bioreactors, and its products include the cholesterol drug Repatha, the bone-building drug Evenity, and the severe asthma drug Tezspire. It earns money by selling these medicines, mostly through large drug wholesalers that supply hospitals and pharmacies. Amgen was founded in 1980 and is based in Thousand Oaks, California.

Company size
10,001+
Company stage
IPO
Headquarters
Thousand Oaks, CA
Founded
1980

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