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