Trainee Medical Writer London

We’re committed to bringing passion and customer focus to the business.

Position Responsibilities

• Manuscripts, abstracts and posters that communicate real‑world evidence. This evidence may be clinical, health economic, statistical or derived from patient‑engagement studies.
• Global or US‑focused value dossiers (global value dossiers (GVDs) and Academy of Managed Care Pharmacy (AMCP) dossiers).
• Value frameworks (value propositions or value briefs) including a hierarchy of messaging and visualization of data.
• Objection handlers.
• Early scientific advice briefing books, and (potentially) health technology assessment (HTA) submissions.

The role will involve the following tasks:

• Conducting targeted literature searches using multiple databases, including PubMed and EMBASE.
• Conducting general desk research including review of clinical guidelines, epidemiology sources, treatment algorithms, 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 is aligned with company and client expectations and with external templates, including those of health technology assessment (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, eagerly, but with appropriate caution.

Position Requirements

• PhD in a life science subject.
• Strong oral and written communication skills in English language.
• Hunger to pioneer use of appropriate AI technologies and methods.
• Ability and knowledge in use of 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 is welcomed.
• 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.

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