Information Specialist

Dexcom • Remote California, CA

19h • $100,700 - $167,900 • Remote

About The Position

The Company Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health. We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us. Meet the team: Join a collaborative Medical Affairs team focused on delivering high-quality, evidence-based insights that support both regulatory success and internal decision-making. As an Information Specialist, you’ll play a critical role at the intersection of science, research, and strategy—partnering with colleagues across Scientific Communications, Regulatory Affairs, and Clinical teams worldwide. In this role, you’ll be the go-to expert for systematic literature searches, evidence organization, and article management, ensuring all outputs are comprehensive, reproducible, and inspection-ready. Your work will directly support regulatory filings and help shape how evidence is used across global teams. You’ll thrive in this team if you enjoy bringing structure to complex information, improving processes, and ensuring quality at every step. With a strong focus on collaboration and continuous improvement, the team is committed to enhancing efficiency, strengthening internal capabilities, and maintaining the highest standards of compliance and scientific rigor.

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

Nice To Haves

• Familiarity with leveraging AI tools to enhance literature search efficiency, screening, and evidence summarization

Responsibilities

• 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.

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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level