Senior Clinical Research Associate

🔥 0 minutes ago

⛰️ Colorado – Remote

⛰️ Colorado – Remote

💵 $100.7k - $167.9k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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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 • Collaborate cross-functionally to ensure on-time monitoring and audit readiness at sponsor and sites • Contribute to study reports and regulatory submission deliverables • Interact professionally and build relationships with Investigators, site staff, Institutional Review Boards (IRBs), and key opinion leaders • Develop study documentation • Perform site selection and qualification • Train and support sites in study procedures • Monitor study compliance and perform study closeout activities • Coordinate with monitors and data management to ensure data quality and timeliness • Contribute to process improvements across clinical study operations

🎯 Requirements

• Bachelor’s degree in a technical discipline and a minimum of 5–8 years related experience, or Master’s degree and 2–5 years equivalent industry experience, or PhD and 0–2 years’ experience • Ability and judgment to work under minimal supervision to plan and execute site study operations • Ability to communicate effectively with site staff, Principal Investigators, and internal study team members • Experience working cross-functionally to achieve goals • Strong Good Clinical Practice (GCP) and clinical study background, including experience as a CRA • Ability to work on multiple studies concurrently and work successfully with monitors • 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 • Willingness 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 • An exciting and innovative, industry-leading organization committed to employees, customers, and communities