Senior Associate- Global HEOR, Value Writing

Job description

Career Category Health Economics Job Description Senior Associate: Global HEOR Value Writing 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 Senior Associate 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 team lead and Global HEOR Product Leads to ensure alignment with product strategy. The Value Writing Senior Associate 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 as assigned by team lead 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. Conduct end to end HTA grade SLRs, TLRs, evidence summaries 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. Review and QC work of peers Contribute to Knowledge sharing sessions 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: +3 years for Master’s degree and +5years 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. .