×
Register Here to Apply for Jobs or Post Jobs. X

Clinical Trial Coordinator; Entry Senior Cardiology

Job in Aurora, Arapahoe County, Colorado, 80012, USA
Listing for: University of Colorado
Full Time position
Listed on 2026-02-20
Job specializations:
  • Healthcare
    Clinical Research, Medical Technologist & Lab Technician
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Open Rank Clinical Trial Coordinator (Entry Senior) Cardiology

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

Why Join Us Why work for the University?
  • 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

Qualifications

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.

Intermediate 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.

  • One (1) year clinical research or related experience.

Senior 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.

  • Two (2) years clinical research or related experience.

Preferred Qualifications
  • 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, Skills, and Abilities
  • 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.

Applicants must be legally authorized to work in the United States without requiring sponsorship. We are unable…

Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary