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MEDICAL WRITER – CLINICAL CONTENT & HEALTH ECONOMICS AND OUTCOMES RESEARCH (HEOR), CLINICAL CONTENT CREATION GROUP
Job Responsibility
Author and support complex scientific deliverables including abstracts, posters, manuscripts, oral presentations, publication extenders, response documents, and white papers across therapeutic areas
Develop medical information content such as standard response letters, FAQs, and customer-facing materials
Draft, edit, and review HEOR-related outputs including value dossiers, slide decks, economic evidence materials, and submissions
Conduct comprehensive literature searches and systematic or targeted reviews to support clinical and HEOR narratives
Partner with health economists, TA researchers, analysts, and statisticians to accurately interpret and translate data from clinical studies, real-world evidence, cost-effectiveness analyses, and budget impact models
Support preparation and submission of content for peer-reviewed journals and scientific congresses
Ensure adherence to publication standards and best practices (e.g., GPP, ICMJE, ISMPP) throughout the content lifecycle
Ensure all materials comply with client policies and external regulatory and ethical guidelines (e.g., FDA/EMA, AMA style)
Maintain high standards for accuracy, consistency, and scientific integrity across all deliverables
Collaborate cross-functionally with internal creative, editorial, medical, and strategic partners
Manage multiple concurrent projects while meeting timelines, quality expectations, and stakeholder needs
Provide flexible writing support across group initiatives as priorities evolve
Requirements
PharmD or advanced scientific degree or bachelor's degree in life sciences, pharmacy, public health, health economics, or related field with relevant experience
1–3+ years of experience in medical writing, medical communications, pharma, consultancy, or related environment
HEOR experience preferred
Strong scientific literacy with the ability to interpret and synthesize clinical, medical, and economic data
Excellent writing and editing skills tailored to both scientific and non-scientific audiences
Knowledge of clinical research processes, publication practices, and regulatory standards
Strong attention to detail, organization, and ability to work independently within cross-functional teams
Proficiency with standard authoring and reference tools (e.g., Microsoft Office, Endnote, Adobe Acrobat)