Information Specialist

Overview Information Specialist in the Medical Affairs team focused on delivering high‑quality, evidence‑based insights that support regulatory success and internal decision‑making. Responsibilities Lead regulatory literature search strategy and execution for key submissions (SOTA, CER), ensuring outputs are comprehensive, traceable, and aligned with submission timelines. Ensure audit‑ready documentation and compliance by applying industry standards (e.g., PRISMA) and maintaining clear records of methodologies, search strategies, and inclusion/exclusion criteria. Manage end‑to‑end reference and article lifecycle, including procurement, tracking, deduplication, version control, and library organization within enterprise systems (EndNote/Distiller). Collaborate cross‑functionally with Scientific Communications, Regulatory Affairs, Clinical, and global Medical Affairs teams to deliver high‑quality, evidence‑based support. Develop concise evidence summaries and respond to complex information requests, enabling consistent, accurate use of data across internal and regulatory materials. Drive process improvements and knowledge management, enhancing efficiency, scalability, and internal ownership of literature and evidence activities currently supported by external vendors. Qualifications Proven experience conducting structured literature searches using biomedical databases such as PubMed/MEDLINE and Embase in pharmaceutical, medical device, or clinical environments. Proficiency with reference management tools and article tracking systems (EndNote/Distiller) to maintain organized, accurate evidence libraries. Exceptional attention to detail with the ability to manage complex data sets and ensure accuracy, traceability, and consistency. Solid organizational and time‑management skills to handle multiple priorities and deadlines in a fast‑paced environment. Familiarity with leveraging AI tools to enhance literature search efficiency, screening, and evidence summarization (preferred). Benefits & Compensation Salary range: $100,700.00 – $167,900.00. A full and comprehensive benefits program. Growth opportunities on a global scale. Access to career development through in‑house learning programs and tuition reimbursement. Travel required: 0‑5%. Travel Required 0‑5%. Experience and Education Requirements Typically requires a Bachelor’s degree and a minimum of 5‑8 years of related experience. Remote Workplace Your location will be a home office; you are not required to live within commuting distance of your assigned Dexcom site (typically 75 miles/120km). If you reside within commuting distance, a hybrid working environment may be available. Ask about our Flex workplace option. Equal Opportunity Statement An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. #J-18808-Ljbffr 1 DexCom Inc