Sr Clinical Research Associate

Meet the team:

Join a collaborative and mission-driven Clinical team dedicated to advancing innovative technologies that improve lives. 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. If you enjoy balancing critical thinking with meaningful patient interaction and want to directly contribute to high-impact clinical programs, this is a team where your work truly makes a difference.

Where you come in:

• As a Sr CRA, you will support execution of clinical studies to support product development and validation while building strong relationships with clinical trial sites.
• You will collaborate cross-functionally to ensure on-time monitoring, audit-readiness both at sponsor and sites, and will contribute to study reports and regulatory submission deliverables.
• You will collaborate effectively with peers and leadership across departments and professionally interact/build relationships with Investigators and site staff, Institutional Review Boards (IRBs), and key opinion leaders.
• You will 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.
• You will coordinate with monitors and data management to ensure data quality and timeliness.
• You will contribute to process improvements across all aspects of clinical study operations.

What makes you successful:

• Ability and judgement to work under minimal supervision to plan and execute site study operations, including on-site and remote training & support, requesting and tracking supplies, documentation, training sites and fellow team members, and generating progress reports.
• 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.

What you’ll get:

• 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.

Travel Required:

• 15-25%

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.

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. Ask about our Flex workplace option.

Please note: The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Dexcom’s AAP may be viewed upon request by contacting Talent Acquisition at [email protected].

If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact Dexcom Talent Acquisition at [email protected].

Meritain, an Aetna Company, creates and publishes the Machine-Readable Files on behalf of Dexcom. To link to the Machine-Readable Files, please click on the URL provided: https://health1.meritain.com/app/public/#/one/insurerCode=MERITAIN_I&brandCode=MERITAINOVER/machine-readable-transparency-in-coverage?reportingEntityType=TPA_19874&lock=true

AI in Hiring Notice: We may use AI supported tools to help make our hiring process more efficient, consistent, and accessible for candidates around the world. All hiring decisions are made by people.

Salary:

$100,700.00 - $167,900.00