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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:
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
- 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
- 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