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