• Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational scale. • In-house based position, responsible for the design and oversight of project monitoring services including training, site/patient recruitment, site data/document management, monitoring project site budgets and regulatory filings that aligns with SOPs, study guidelines and GCP best practices. • In the function of Lead CRA, will act as primary liaison between CRAs and project team and may be required to participate in the development of project plans, protocols, CRFs, communications or other monitoring forms, documents and tools. • Represents the corporation by maintaining collaborative relationships with stakeholders.

• Lead the design and execution of qualitative and mixed-methods research to tackle complex behavioral, clinical, and product-related questions across Dexcom’s portfolio. • Facilitate qualitative research activities, including moderating focus groups, conducting interviews, and observing participant behavior to ensure the collection of rich, meaningful data. • Utilize health behavior change models (e.g., COM-B, Self-Determination Theory) to inform study design, data analysis, and interpretation. • Analyze qualitative data using advanced methodologies and integrate findings with quantitative and digital-health data when applicable. • Convert qualitative findings into clear, actionable insights and recommendations that guide product development, digital experiences, clinical strategies, and patient engagement initiatives. • Act as a strategic partner to cross-functional teams (Product, R&D, Clinical Affairs, Medical Affairs, Marketing), helping them understand behavioral drivers, barriers, and opportunities. • Develop comprehensive research reports and presentations, effectively communicating findings and recommendations to stakeholders at all organizational levels. • Keep abreast of industry trends, methodologies, and best practices in qualitative research, continuously enhancing your skills to provide high-quality insights.

• Conduct in-depth business, market, and technology research on industries, competitors, emerging trends, and potential partners. • Analyze and synthesize complex information into clear executive-ready insights, structured briefs, comparisons, and actionable recommendations. • Produce research-based written content, including analytical articles, thought leadership drafts, and supporting materials based on completed research. • Identify new business opportunities and strategic directions by spotting patterns, market signals, and partnership potential. • Use AI-powered tools to accelerate research, summarization, and information structuring in daily workflows. • Occasionally support business development initiatives with research-driven company profiles, target lists, and outreach context. • Handle selected administrative and organizational tasks (documentation, coordination, light scheduling, vendor communication) as a supplemental responsibility, ensuring smooth execution of priorities.

• Perform and coordinate all aspects of the clinical monitoring and site management process • Conduct on-site or remote visits to assess protocol and regulatory compliance • Manage procedures and guidelines from different sponsors and/or monitoring environments • Ensure the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs • Ensure audit readiness and develop collaborative relationships with investigational sites and client company personnel • Assist the project manager or clinical team manager on assigned projects • Mentor and train junior clinical team members