Senior Clinical Research Associate - Remote (CGM/Devices)

Dexcom; United States; Hybrid; USD 101.000 - 168.000; Vollzeit

Benefits dieser Stelle

Life changing CGM technology

Comprehensive benefits

Global growth opportunities

In-house learning programs

Industry-leading organization

Zusammenfassung

Dexcom invites a Sr. Clinical Research Associate to join our clinical team supporting CGM product development. You will manage studies from protocol through patient recruitment, consent, screening, and visit execution, partnering with sites and cross-functional teams.

The role emphasizes GCP compliance, data quality, and timely study deliverables in a fast-paced environment, with remote/hybrid work options and ongoing professional growth.

Qualifikationen

• Bachelor degree in a technical discipline; advanced degrees optional
• 5–8 years related experience or Master’s degree with 2–5 years; PhD with 0–2 years acceptable
• Strong GCP and clinical study background; CRA experience preferred
• Experience in medical device industry and/or diabetes is a plus
• Ability to work on multiple studies concurrently and collaborate cross-functionally

Aufgaben

• Support execution of clinical studies to support product development and validation.
• Build relationships with clinical trial sites and monitor study progress.
• Prepare study documentation, site qualification, and training.
• Ensure data quality and timeliness with monitors and data management.
• Contribute to regulatory submission deliverables and study reports.

Kenntnisse

Cross-functional collaboration

GCP experience

CRA experience

Clinical trial coordination

Communication skills

Ausbildung

Bachelor's degree in a technical discipline

Master’s degree in related field

PhD in relevant field

Tools

EDC systems

CTMS

eTMF

Jobbeschreibung

Dexcom invites a Sr. Clinical Research Associate to join our clinical team supporting CGM product development. You will manage studies from protocol through patient recruitment, consent, screening, and visit execution, partnering with sites and cross-functional teams.

The role emphasizes GCP compliance, data quality, and timely study deliverables in a fast-paced environment, with remote/hybrid work options and ongoing professional growth.