Information Specialist

🕒 May 28

🏄 California – Remote

🏄 California – Remote

💵 $100.7k - $167.9k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

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Dexcom

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1999

⚕️ Healthcare Insurance

🧬 Biotechnology

Healthcare Insurance • Biotechnology • Wearable Technology

Dexcom is a leading provider of continuous glucose monitoring (CGM) systems, revolutionizing how people manage diabetes and track their glucose levels. Known for their best-in-class glucose biosensing technology, Dexcom offers products like the Dexcom G7 CGM system, which provides real-time glucose monitoring and insights to help individuals become healthier. Founded in 1999, Dexcom has consistently innovated in the field of diabetes management, empowering users to take control of their health with accurate and advanced glucose monitoring solutions. Their products are designed for both adults and children and do not require a prescription.

📋 Description

• Lead regulatory literature search strategy and execution for key submissions (e.g., 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 (e.g., 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.

🎯 Requirements

• Proven experience conducting structured literature searches using biomedical databases such as PubMed/MEDLINE and Embase • Background supporting systematic literature reviews, regulatory submissions, or clinical evaluations within pharmaceutical, medical device, or clinical environments • Proficiency with reference management tools and article tracking systems to maintain organized, accurate evidence libraries • Strong ability to collaborate effectively with cross-functional and global teams across Medical Affairs, Regulatory, and Clinical functions • 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

• A front row seat to life changing CGM technology. • Learn about our brave #dexcomwarriors community. • A full and comprehensive benefits program. • Growth opportunities on a global scale. • Access to career development through in-house learning programs and/or qualified tuition reimbursement. • An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.