Dexcom · 13 hours ago
Sr Staff Clinical Program Manager
United States
Full-time
Onsite
Senior Level, Lead/Staff
$135K/yr - $225K/yr
8+ years expDexcom Corporation is a pioneer and global leader in continuous glucose monitoring (CGM), aiming to improve health outcomes through innovative technology. The Sr. Staff Clinical Program Manager will lead global clinical programs, translating product strategy into actionable plans while ensuring compliance with regulatory requirements and operational excellence.
DiabetesHealth DiagnosticsMedical DeviceSensor
Responsibilities
Serve as the clinical program leader for one or more global, cross‑functional core teams—translating product strategy into executable clinical program plans and ensuring alignment with broader technical, regulatory, and business objectives
Define and drive the clinical program roadmap, including strategy, requirements, milestones, and interdependencies across multiple complex studies
Lead global study teams through all phases of execution—from early design and feasibility through study close‑out—ensuring scientific rigor, operational excellence, and compliance with worldwide Good Clinical Practice (GCP), ISO 14155, and other regional regulatory requirements
Interface at a senior level with Executive Management, R&D, Regulatory Affairs, Quality, Operations, Marketing, and external partners/CROs to ensure technical and operational integration across program components
Operationalize global clinical strategies, including study design approaches, regulatory evidence pathways, and site/country selection strategies informed by regional regulatory landscapes
Oversee and manage complex program budgets, financial forecasting, and global resource allocation, ensuring optimal use of internal/external resources
Establish and monitor KPIs for clinical execution, proactively identifying risks to study startup, enrollment, data quality, regulatory compliance, and program timelines—and driving mitigation strategies across global teams
Lead vendor strategy and governance, including CRO and specialized vendor selection, contract oversight, performance management, and escalation resolution for multi‑region programs
Implement innovative operational models and tools to optimize efficiency, quality, and scalability of global clinical execution (e.g., digital trial capabilities, centralized monitoring approaches, risk‑based quality management)
Represent the clinical program externally, providing senior‑level engagement with investigators, global KOLs, regulatory bodies (as appropriate), and other external stakeholders to ensure alignment on scientific and regulatory expectations
Ensure integration of clinical insights into product development, partnering closely with R&D and technical program management teams to translate clinical outcomes into product improvements and future evidence needs
Qualification
Required
You have a strong regulatory knowledge, including Good Clinical Practices (GCPs) and ISO 14155
You have experience with protocol, ICF, CRF development
You have experience with global clinical study planning and execution in the medical device industry
You have experience serving as a Clinical representative on a product development core team
You have exceptional organizational skills and ability to deal with competing priorities, also strong reasoning and problem-solving ability
You have excellent communication (written and verbal) and presentation skills along with leadership qualities
You have strong interpersonal skills and ability to work effectively on cross-functional & global teams
You thrive in an extremely fast-paced environment
Typically requires a Bachelor's degree in a technical discipline, and a minimum of 13+ years related experience or a Master's degree and 8+ years equivalent industry experience of a PhD and 5+ years of experience
Preferred
Successful experience managing outside CRO groups in Class II/III, preferably diabetes, device studies
Proficient with MS Office Suite (Excel, Word and PowerPoint), MS Project, and Smartsheet
Benefits
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.
Company
Dexcom
Dexcom develops, manufactures, and distributes continuous glucose monitoring systems for diabetes management.
10001+ employees
H1B Sponsorship
Dexcom has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (54)
2024 (41)
2023 (67)
2022 (75)
2021 (49)
2020 (36)
Funding
Current Stage
Public CompanyTotal Funding
$2.16BKey Investors
RWI Group
2023-05-02Post Ipo Debt· $1B
2020-05-12Post Ipo Debt
2018-11-01Post Ipo Equity· $750M
Leadership Team
Jacob Leach
Chief Operating Officer
Matt Dolan
Executive Vice President, Strategy, Corporate Development & Dexcom Labs
Recent News
2026-01-16
Medical Device Network
2026-01-15
Company data provided by crunchbase