
Job Overview
Location
Remote - United States
Job Type
Full-time
Category
Software Engineering
Date Posted
June 18, 2026
Full Job Description
đź“‹ Description
- • Serve as a key contributor to Dexcom’s Global Medical Affairs team by providing medical and clinical review of promotional materials for CGM, biosensors, diabetes, and metabolic disease-related content in the U.S., Canada, and other English-speaking regions.
- • Collaborate with cross-functional teams including Regulatory, Marketing, Medical Writing, Scientific Communications, Clinical Affairs, Evidence Planning, and Legal to ensure accurate, compliant, and traceable marketing claims across digital and collateral materials.
- • Actively participate in the North American Promotional Material Review Team (PMRT) and the Global Medical Review Committee (MRC) to evaluate and approve promotional content using the Veeva Promotional Materials Review platform.
- • Maintain current knowledge of clinical literature on glucose management, diabetes, metabolic disease, and CGM technologies, proactively identifying emerging data and Standards of Care for commercial utilization.
- • Review and interpret clinical studies to assess methodology, outcomes, strengths, and limitations, translating findings into accurate medical claims for promotional use.
- • Update and maintain product and marketing claims matrices globally and regionally, ensuring alignment with regulatory guidance from the FDA, Health Canada, and other relevant bodies.
- • Support the development and standardization of Standard Operating Procedures (SOPs) for Medical Affairs functions, particularly within promotional review and medical inquiry subfunctions.
- • Respond to medical inquiries from healthcare professionals in the U.S., Canada, and other English-speaking regions, providing evidence-based, compliant responses.
- • Conduct monthly reporting on promotional review metrics and key performance indicators to track efficiency and compliance within the Medical Affairs function.
- • Perform internal audits of claims utilization in promotional materials and collaborate with Regulatory and Legal teams to identify areas for process improvement.
- • Communicate clearly and effectively with commercial teams to explain rationale for changes to promotional content, ensuring alignment on medical accuracy and regulatory compliance.
- • Stay current on U.S. and Canadian regulatory guidance regarding health and product claims creation, implementation, and documentation.
- • Utilize Microsoft Office Suite (Word, Excel, PowerPoint), Adobe Acrobat Pro, Microsoft 365, Smartsheet, Microsoft Copilot, and Microsoft Teams daily to execute responsibilities.
- • Work independently with minimal supervision while managing multiple concurrent projects in a fast-paced, evolving environment.
- • Apply problem-solving skills to identify efficiencies and innovations within the Medical, Legal, and Regulatory review process.
- • Adhere to Dexcom’s core values: Think Big, Be Dependable, Listen and Serve with Integrity, in all interactions and deliverables.
- • Travel up to 15–25% to support team meetings, training, and cross-functional initiatives.
🎯 Requirements
- • Bachelor’s degree in a science-related field with 5–8 years of related experience
- • Clinical registration or licensure as RD, RN, PharmD, or advanced degree (Master’s or PhD) or fellowship in a science-related field
- • Demonstrated knowledge of diabetes literature, management, and the pharmaceutical/medical device industry in the U.S. and Canada
- • Experience with clinical study methodology, scientific literature review, and translation of clinical evidence into promotional claims
- • Proficiency in Veeva Promotional Materials and Medical Communications platforms
- • Strong attention to detail, organizational skills, and ability to multitask in a fast-paced environment
🏖️ Benefits
- • Comprehensive benefits program
- • Growth opportunities within Medical Affairs
- • Access to in-house learning programs and qualified tuition reimbursement
- • Front-row access to life-changing CGM technology and the #dexcomwarriors community
- • Opportunity to work in an innovative, industry-leading organization committed to employee and community impact
- • Hybrid work flexibility available if residing within 75 miles/120km of a Dexcom site
Skills & Technologies
See exactly how your profile matches this role — strengths, skill gaps, and what to do about them.
About DexCom, Inc.
DexCom, Inc. develops, manufactures, and distributes continuous glucose monitoring (CGM) systems for diabetes management. Its sensors, transmitters, and software provide real-time glucose data to patients and healthcare providers. The company serves insulin-intensive diabetes populations worldwide.
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