Senior Clinical Research Associate - Remote CGM Trials

1 DexCom Inc; Colorado; Hybrid; USD 101,000 - 168,000; Full time

Benefits offered by this job

Comprehensive benefits program

Global growth opportunities

Tuition reimbursement

Career development programs

Dexcom warrior community

Job summary

Dexcom is seeking a Sr. Clinical Research Associate (CRA) to lead hands-on clinical studies from protocol development to site execution. You will build strong relationships with trial sites, IRBs, and investigators while ensuring timely monitoring and regulatory deliverables.

The role requires GCP expertise, experience in clinical trials, and familiarity with CGM systems and diabetes studies. Travel and a hybrid remote work setup are involved, with a comprehensive benefits program.

Qualifications

• Typically requires a 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 a PhD and 0 – 2 years’ experience.
• Experience with CGM systems and diabetes clinical trials is a plus.
• Strong Good Clinical Practice (GCP) and clinical study background.
• Experience with using electronic data capture systems (EDC), Clinical Trial Management Systems (CTMS), and electronic trial master files (eTMF).
• Ability to communicate effectively with site staff and internal study team members and cross-functional teams.

Responsibilities

• Support execution of clinical studies to support product development and validation.
• Collaborate cross‑functionally to ensure on‑time monitoring and audit-readiness both at sponsor and sites.
• Collaborate effectively with peers and leadership across departments and interact with Investigators and site staff, IRBs, and key opinion leaders.
• Develop study documentation, perform site selection/qualification, train and support sites in study procedures, monitor study compliance, study closeout, and other activities.
• Coordinate with monitors and data management to ensure data quality and timeliness.
• Contribute to process improvements across all aspects of clinical study operations.

Skills

GCP knowledge

CRA experience

diabetes knowledge

cross-functional collaboration

EDC/CTMS experience

Education

Bachelor’s degree in technical discipline

Master’s degree (related field)

PhD in related field

Tools

EDC

CTMS

eTMF

Job description

Dexcom is seeking a Sr. Clinical Research Associate (CRA) to lead hands-on clinical studies from protocol development to site execution. You will build strong relationships with trial sites, IRBs, and investigators while ensuring timely monitoring and regulatory deliverables.

The role requires GCP expertise, experience in clinical trials, and familiarity with CGM systems and diabetes studies. Travel and a hybrid remote work setup are involved, with a comprehensive benefits program.