Senior Clinical Research Associate

Dexcom

Senior Clinical Research Associate supporting Dexcom’s continuous glucose monitoring clinical studies. Managing site operations, monitoring, compliance, documentation, and regulatory deliverables.

Posted 8/13/2026full-timeRemote • 🇺🇸 United StatesSenior💰 $100,700 - $167,900 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical study operations, including site selection, training, and compliance monitoring, while effectively collaborating with cross-functional teams and maintaining strong relationships with clinical trial sites.

Highest-signal resume keywords

Clinical Research Associate ExperienceGood Clinical Practice (GCP)Electronic Data Capture Systems (EDC)Clinical Trial Management Systems (CTMS)Diabetes Clinical Trials Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Site SelectionStudy Documentation DevelopmentStudy Compliance MonitoringProgress Report GenerationStudy Closeout Conduct

Soft Skills

Effective CommunicationRelationship BuildingJudgment Under Minimal Supervision

Tools & Technologies

Electronic Trial Master Files (eTMF)Continuous Glucose Monitoring (CGM) Systems

Industry Keywords

Clinical TrialsInsulin TherapiesInsulin PumpsDigital Health TechnologiesCross-Functional Collaboration

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Support execution of clinical studies for product development and validation
Build strong relationships with clinical trial sites
Ensure on-time monitoring and audit-readiness at the sponsor and sites
Contribute to study reports and regulatory submission deliverables
Collaborate with peers and leadership across departments
Interact professionally with Investigators, site staff, Institutional Review Boards, and key opinion leaders
Develop study documentation
Perform site selection and qualification
Train and support sites in study procedures
Monitor study compliance and conduct study closeout
Coordinate with monitors and data management to ensure data quality and timeliness
Contribute to process improvements across clinical study operations
Plan and execute site study operations with minimal supervision
Request and track supplies, documentation, and training
Generate progress reports
Work on multiple studies concurrently and reduce time from last participant to database lock while improving site compliance

Requirements

What you’ll need

Bachelor’s degree in a technical discipline and 5–8 years of related experience, or Master’s degree and 2–5 years of equivalent industry experience, or PhD and 0–2 years’ experience
Ability and judgment to work under minimal supervision
Experience planning and executing site study operations, including on-site and remote training and support
Ability to request and track supplies and documentation
Ability to train sites and fellow team members and generate progress reports
Effective communication with site staff, Principal Investigators, and internal study team members
Cross-functional work experience
Strong Good Clinical Practice (GCP) and clinical study background
Experience as a Clinical Research Associate
Ability to work on multiple studies concurrently
Ability to work successfully with monitors to reduce time from last participant on study to database lock and improve site compliance
Experience using electronic data capture systems (EDC), Clinical Trial Management Systems (CTMS), and electronic trial master files (eTMF)
Preferred experience with Continuous Glucose Monitoring (CGM) Systems
Preferred experience in diabetes clinical trials involving insulin therapies, insulin pumps, or digital health technologies
Ability to travel 15–25%

Benefits

Comp & perks

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
Home office workplace
Flex workplace option may be available
Equal Opportunity Employer
Reasonable accommodations for individuals with disabilities