Sr Clinical Research Associate

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 and mission-driven Clinical team dedicated to advancing innovative technologies that improve lives. As a Sr. Clinical Research Associate (CRA), you will play a hands-on role in bringing clinical studies to life—from protocol and document development to patient recruitment, consent, screening, and study visit execution. This team thrives on curiosity, precision, and creative problem-solving, and values individuals who bring both structure and flexibility to a fast-paced research environment. If you enjoy balancing critical thinking with meaningful patient interaction and want to directly contribute to high-impact clinical programs, this is a team where your work truly makes a difference. Where you come in: As a Sr CRA, you will support execution of clinical studies to support product development and validation while building strong relationships with clinical trial sites. You will collaborate cross-functionally to ensure on-time monitoring, audit-readiness both at sponsor and sites, and will contribute to study reports and regulatory submission deliverables. You will collaborate effectively with peers and leadership across departments and professionally interact/build relationships with Investigators and site staff, Institutional Review Boards (IRBs), and key opinion leaders.  You will develop study documentation, perform site selection/qualification, train and support sites in study procedures, monitor study compliance, study closeout, and other activities related to study operations. You will coordinate with monitors and data management to ensure data quality and timeliness. You will contribute to process improvements across all aspects of clinical study operations. What makes you successful: Ability and judgement to work under minimal supervision to plan and execute site study operations, including on-site and remote training & support, requesting and tracking supplies, documentation, training sites and fellow team members, and generating progress reports. Ability to communicate effectively with site staff, including Principal Investigators, and internal study team members. Skill and experience at working cross-functionally to achieve goals. Strong Good Clinical Practice (GCP) and clinical study background, including experience as a CRA; experience in the medical device industry and/or with diabetes is a plus. Ability to work on multiple studies concurrently and to work with monitors successfully to reduce overall time from last participant on study to database lock while improving site compliance. Experience with using electronic data capture systems (EDC), Clinical Trial Management Systems (CTMS), and