Trainee Medical Writer London

Responsibilities

Under the guidance of an experienced medical writer, assist in the development of a wide range of materials that support value demonstration and reimbursement strategies for pharmaceuticals, medical devices, and potentially digital technologies. These materials include manuscripts, abstracts, posters, value dossiers (global value dossiers and AMCP dossiers), value frameworks (value propositions or value briefs), objection handlers, early scientific advice briefing books, and, potentially, health technology assessment (HTA) submissions.

• Conducting targeted literature searches using multiple databases, including PubMed and EMBASE.
• Conducting general desk research, including review of clinical guidelines, epidemiology sources, treatment algorithms, and health technology assessment reports.
• Analyzing, interpreting, and synthesizing scientific, medical, health economic, and statistical publications and reports, including economic model reports and statistical analysis plans.
• Collaborating with cross‑functional teams, including consultants, health economists, and senior writers.
• Writing scientifically accurate, clear, and publication‑grade content that aligns with company and client expectations and external templates, such as those of HTA agencies.
• Supporting execution of primary research programs (e.g., focus groups, interviews) by preparing discussion guides to pressure‑test and inform value story development.
• Using appropriate and evolving AI methods with caution and appropriate oversight.

Requirements

• PhD in a life science subject.
• Strong oral and written communication skills in English.
• Hunger to pioneer the use of appropriate AI technologies and methods.
• Ability and knowledge in using PubMed/Medline, Google Scholar, and other literature research platforms.
• Proficiency in MS Office Suite (Microsoft Word, PowerPoint, Outlook) and reference management software (e.g., EndNote).
• General understanding of clinical research design and applicable standards and regulations for clinical trials (welcome).
• High attention to detail with superior organizational and time‑management skills.
• Strong team player, ability to work with cross‑functional staff.
• Ability to work under the pressure of deadlines and manage multiple priorities.

#J-18808-Ljbffr…