[Hiring] Senior Clinical Research Associate @Dexcom

Role Description

As a Sr. Clinical Research Associate (CRA), you will play a hands-on role in bringing clinical studies to life—from protocol and document development to patient recruitment, consent, screening, and study visit execution. This team thrives on curiosity, precision, and creative problem-solving, and values individuals who bring both structure and flexibility to a fast-paced research environment.

Where you come in:

• Support execution of clinical studies to support product development and validation while building strong relationships with clinical trial sites.
• Collaborate cross-functionally to ensure on-time monitoring, audit-readiness both at sponsor and sites, and contribute to study reports and regulatory submission deliverables.
• Professionally interact/build relationships with Investigators, site staff, Institutional Review Boards (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 related to study operations.
• Coordinate with monitors and data management to ensure data quality and timeliness.
• Contribute to process improvements across all aspects of clinical study operations.

Qualifications

• Ability and judgement to work under minimal supervision to plan and execute site study operations.
• Ability to communicate effectively with site staff, including Principal Investigators, and internal study team members.
• Skill and experience at working cross-functionally to achieve goals.
• Strong Good Clinical Practice (GCP) and clinical study background, including experience as a CRA; experience in the medical device industry and/or with diabetes is a plus.
• Ability to work on multiple studies concurrently and to work with monitors successfully to reduce overall time from last participant on study to database lock while improving site compliance.
• Experience with 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.

Benefits

• A front row seat to life changing CGM technology.
• Learn about our brave #dexcomwarriors community.
• 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 our employees, customers, and the communities we serve.

Experience and Education Requirements

• 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.

Travel Required

• 15-25%

Remote Workplace

• Your location will be a home office; you are not required to live within commuting distance of your assigned Dexcom site (typically 75 miles/120km).
• If you reside within commuting distance of a Dexcom site (typically 75 miles/120km) a hybrid working environment may be available.