Clinical Trial Coordinator; Entry – Senior Cardiology
Listed on 2026-09-23
-
Research/Development
Clinical Research -
Healthcare
Clinical Research
University of Colorado Anschutz Medical Campus
Department:
Medicine – Division of Cardiology
Job Title: Open Rank Clinical Trial Coordinator (Entry – Senior)– Cardiology
Position #: – Requisition # 41145
Job SummaryClinical Science Professionals perform clinical research related functions which may include patient-oriented research or research conducted with human subjects. Patient-oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new technologies. Clinical Science Professionals may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research.
We are seeking a Clinical Trial Coordinator in the areas of interventional cardiology and imaging research, electrophysiology, and heart failure. This position will support multiple Industry Supported Clinical Trials, Federally Funded Clinical Trials, and Investigator-Initiated Clinical Trials. This position focuses primarily on the responsibility of data collection, interpretation and documentation of clinical research data, and meeting with research patients for study-related purposes.
The amount of time spent on required tasks may shift depending on the needs of the department.
- Abstracts and records all patient data essential to the study onto required Case Report Forms (CRFs) and into the Clinical Trials database, as needed, in an accurate and timely fashion.
- Ensures complete source documentation is compiled in research records.
- Schedules and tracks submission of prescreening, screening and enrollment logs as required by study sponsor.
- Obtains and reviews the electronic medical records via EPIC for the identifying and screening of potential research subjects.
- Gather and maintain source documents, regulatory binders, and subject binders.
- Ensures that the current version of consent forms are completed, and that the informed consent process is properly documented and filed.
- Review medical history to determine eligibility status.
- Schedules, coordinates, prepares for and conducts sponsor monitor visits and audits in collaboration with the regulatory team, CRC, and other team members.
Onsite – this role is expected to work onsite and is located in Aurora, Colorado.
Why Join UsJoin a dynamic and mission-driven team at the forefront of advancing cardiovascular medicine. Our cardiology clinical trial team partners with top investigators and leading industry sponsors to bring innovative treatments and cutting-edge research to patients who need it most. Every day, your work will contribute directly to improving patient outcomes and shaping the future of heart health.
You’ll be supported by a collaborative, experienced team that values professional growth, mentorship, and a strong work-life balance. Whether you’re just starting your research career or looking to deepen your expertise, this is a place where your contributions are meaningful, your voice is heard, and your impact is real.
Why work for the UniversityWe have AMAZING benefits and offer exceptional amounts of holiday,vacation, and sick leave! The University of Colorado offers an excellent benefits package including:
- Medical:
Multiple plan options - Dental:
Multiple plan options - Additional Insurance:
Disability, Life, Vision - Retirement 401(a) Plan:
Employer contributes 10% of your gross pay - Paid Time Off:
Accruals over the year - Vacation Days: 22/year (maximum accrual 352 hours)
- Sick Days: 15/year (unlimited maximum accrual)
- Holiday Days: 15/year
- Tuition Benefit:
Employees have access to this benefit on all CU campuses - ECO Pass:
Reduced rate RTD Bus and light rail service
There are many additional perks & programs with the CU Advantage.
QualificationsMinimum Qualifications Entr…
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