Global HEOR Systematic Literature Review Senior Associate

11 hours ago

Hyderabad, Telangana, India Amgen Inc Full time ₹ 20,00,000 - ₹ 25,00,000 per year

Reports To: Global Systematic Literature Review Team Lead

Position Summary

The Global Systematic Literature Review (SLR) Senior Associate provides expertise in designing, executing, and managing literature review services within Amgens Global HEOR function. The SLR Senior Associate will collaborate closely with team lead and Global HEOR Product Leads to align with HEOR product strategy. This role supports global access to Amgen's therapies through the generation of high-quality, evidence-based outputs across the product lifecycle.

Key Responsibilities

  • Refine literature review questions in alignment with team lead and prepare research protocols.

  • Design literature searches for electronic databases (e.g., PubMed, EMBASE, Cochrane Library) and grey literature (e.g., conference proceedings, regulatory sites).

  • Screen abstracts and full-texts to determine relevance based on PICO criteria.

  • Create and review PRISMA diagrams to document full-text study selection.

  • Extract data from included articles into a predefined data extraction template

  • Draft evidence tables, figures, final reports, and presentation decks, interpreting patterns and trends.

  • Ensure quality of assigned work

  • People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEOR teams across various time zones

Qualifications

Education

  • Bachelors or Masters degree in pharmacy, health economics, public health, medicine, epidemiology, or a related health sciences field.

Experience

  • Years of relevant experience in systematic literature review methods in the pharmaceutical, biotech or consulting setting: +3 years for Masters degree and +5 years for Bachelors degree.

  • Experience of conducting different types of literature reviews (clinical, economic, QoL, burden of illness etc.)

  • Able to prioritize and manage multiple projects with high efficiency in first pass, second pass and data extraction milestones

  • Proficiency in biomedical databases (e.g., MEDLINE, Embase).

  • Strong understanding of research principles and implementation.

Skills & Competencies

  • Excellent English oral and written communication, with ability to tailor content to different stakeholders; past medical writing experience is a plus

  • Skilled with EndNote or other reference management tools (preferred).

  • Proficiency with Microsoft Office (Word, PowerPoint, Excel).

  • Experience on systematic review tools and citation databases (e.g., PubMed, EMBASE);

  • High attention to detail and strong editing/fact-checking abilities.

  • Innovative use of artificial intelligence to boost efficiency

Organizational Behaviors

  • Team-oriented with demonstrated collaboration.

  • Capable of managing multiple projects simultaneously.

  • Comfortable working in a global team across time zones and cultures.

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