#R-240904
port development of Global Value dossiers, AMCP dossiers, EU JCA Dossier, HEOR publications (slide decks, abstracts, posters, manuscripts)
Qualifications
Education
Experience
Years of relevant experience in systematic literature review methods in the pharmaceutical, biotech or consulting setting: +6 years for Master's degree and +8 years for Bachelor's degree.
Experience in evidence synthesis feasibility assessments and network meta-analysis is preferred.
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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