Trainee Medical Writer London

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

Position Responsibilities Under the guidance of an experienced medical writer, to 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:

• 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. These will include 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, PPT, and 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