Senior Clinical Research Associate

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🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $100.7k - $167.9k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

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Dexcom

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1999

🏥 Healthcare

💼 Consulting

🏭 Manufacturing

Healthcare • Consulting • Manufacturing

Dexcom is a leading provider of continuous glucose monitoring (CGM) systems, revolutionizing how people manage diabetes and track their glucose levels. Known for their best-in-class glucose biosensing technology, Dexcom offers products like the Dexcom G7 CGM system, which provides real-time glucose monitoring and insights to help individuals become healthier. Founded in 1999, Dexcom has consistently innovated in the field of diabetes management, empowering users to take control of their health with accurate and advanced glucose monitoring solutions. Their products are designed for both adults and children and do not require a prescription.

📋 Description

• 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

• 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

• 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