Clinical Trial Coordinator; Entry Senior Cardiology
Listed on 2026-02-20
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Healthcare
Clinical Research, Medical Technologist & Lab Technician
Open Rank Clinical Trial Coordinator (Entry Senior) Cardiology Description University of Colorado Anschutz Medical Campus Department:
Medicine - Division of Cardiology
Job Title:
Open Rank Clinical Trial Coordinator (Entry - Senior) - Cardiology Position #: - Requisition #: 39013 Key Responsibilities
Coordinate and support day-to-day clinical trial operations partnering with Principal Investigators and research leadership to ensure studies are conducted efficiently and according to protocol.
Screen, recruit, consent, and educate research participants including reviewing medical records, determining eligibility, conducting study visits, and maintaining accurate screening and enrollment documentation.
Ensure accurate and timely data collection and documentation including abstraction of source data, completion of Case Report Forms (CRFs), and entry into clinical trial databases and the electronic medical record (EPIC).
Maintain compliance with regulatory and institutional requirements including FDA regulations, IRB policies, study protocols, and departmental standard operating procedures.
Manage study logistics and coordination such as scheduling participant visits, coordinating clinical and ancillary services (e.g., labs, imaging, pharmacy), and ensuring study supplies and equipment are available and functional.
Support monitoring visits, audits, and regulatory submissions including preparation for sponsor monitor visits, responding to data queries, and assisting with IRB continuing reviews and study documentation.
Contribute to team success and continuous improvement including training and mentoring junior staff, serving as a primary coordinator on assigned studies, and assisting with process development, study start‑up, and close‑out activities as appropriate to level.
Work Location:
Hybrid
Medical:
Multiple plan optionsDental:
Multiple plan optionsAdditional Insurance:
Disability, Life, VisionRetirement 401(a) Plan:
Employer contributes 10% of your gross payPaid Time Off:
Accruals over the yearVacation 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 campusesECO Pass:
Reduced rate RTD Bus and light rail service
Minimum Qualifications Entry Level
Bachelor’s degree in biology, molecular biology, chemistry, genetics, or related field.
A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year‑for‑year basis.
Bachelor’s degree in biology, molecular biology, chemistry, genetics, or related field.
A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year‑for‑year basis.
One (1) year clinical research or related experience.
Bachelor’s degree in biology, molecular biology, chemistry, genetics, or related field.
A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year‑for‑year basis.
Two (2) years clinical research or related experience.
Bachelor’s degree in science or health related field.
Three (3) years of clinical research or related experience.
Experience with electronic data capture systems (e.g., EMR or EHR and data management systems).
Epic, Oncore, and Redcap training.
Experience with COMIRB, WIRB, or other IRB.
Prior industry clinical trial, EDC, and CTMS experience.
Knowledge and understanding of federal regulations and Good Clinical Practice (GCP).
Ability to communicate effectively, both in writing and orally.
Ability to establish and maintain effective working relationships with employees at all levels throughout the institution.
Outstanding customer service skills.
Knowledge of basic human anatomy, physiology, and medical terminology.
Ability to interpret and master complex research protocol information.
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