Supervisor Clinical Affairs

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 At Dexcom, our mission is to empower people to take control of their health through innovative continuous glucose monitoring technology. The Clinical Affairs team plays a critical role in advancing this mission by generating high-quality clinical evidence that supports product innovation, regulatory compliance, and patient outcomes. As a Clinical Affairs Supervisor, you will lead a team responsible for executing sponsor-investigator clinical studies. You'll have the opportunity to collaborate with cross-functional teams, clinical experts, and key stakeholders while driving operational excellence and continuous improvement within clinical research activities. Where You Come In You will lead and oversee sponsor-investigator clinical studies from study start-up through study close-out. You will supervise and develop a team of Clinical Research professionals responsible for study execution and trial management. You will create and maintain study-related documentation, including source documents, case report forms (CRFs), IRB submissions, clinical training materials, and study tools. You will partner with Clinical Affairs leadership and cross-functional stakeholders to plan, execute, and monitor clinical studies. You will establish and track study timelines, deliverables, and operational milestones to ensure successful trial execution. You will oversee subject recruitment, study visits, regulatory documentation, data collection activities, and study close-out processes. You will ensure studies are conducted in accordance with study protocols, Good Clinical Practice (GCP), ICH Guidelines, applicable regulations, and Dexcom SOPs. You will identify, document, and escalate adverse events, serious adverse events, protocol deviations, and other study risks as required. You will establish performance metrics and quality benchmarks while driving continuous improvement initiatives across clinical operations. You will build and maintain strong working relationships with internal stakeholders, Institutional Review Boards (IRBs), healthcare professionals, regulatory agencies, and key opinion leaders. What Makes You Successful You have a Bachelor's degree in Life Sciences, Nursing, Pharmacy, Healthcare, or a related discipline. You have 10+ years of Clinical Affairs and Clinical Operations experience within the medical device, pharmaceutical, or Clinical Research Organization (CRO) industry. You possess comprehensive knowledge of clinical trial design, Good Clinical Practice (GCP), ICH guidelines, regulatory requirements, quality systems, and risk management practices. You hold an active healthcare practitioner license and are eligible to serve as a