Open Rank Cardiology Clinical Trial Coordinator

University of Colorado System; Aurora (CO); On-site; USD 50,000 - 72,000; Full time

Benefits offered by this job

Health insurance

Tuition benefit

Paid time off

Retirement plan

Job summary

University of Colorado Anschutz Medical Campus in Aurora, CO is seeking an Open Rank Clinical Trial Coordinator (Entry – Senior) in Cardiology. This role supports interventional cardiology and imaging research, electrophysiology, and heart failure, focusing on data collection, interpretation, and documentation for multiple trials.

Responsibilities include CRF data entry, source documentation, enrollment logistics, EMR screening, consent documentation, and coordinating sponsor visits with the

Qualifications

• Bachelor's degree in any field.
• 1 year of clinical research or related experience.
• Two years of clinical research or related experience (senior level).

Responsibilities

• Abstract and record patient data on CRFs and into the Clinical Trials database.
• Ensure complete source documentation in research records.
• Schedule and track prescreening, screening and enrollment logs as required by sponsor.
• Obtain and review EMR/EHR for identifying and screening potential subjects.
• Maintain source documents, regulatory binders, and subject binders.
• Ensure current consent forms are completed and properly documented.
• Review medical history to determine eligibility.
• Coordinate sponsor monitor visits and audits with the regulatory team.

Skills

GCP knowledge

Communication skills

Regulatory compliance

Team collaboration

Education

Bachelor's degree in any field

Tools

EPIC

REDCap

EMR/EHR

CTMS

Job description

University of Colorado Anschutz Medical Campus in Aurora, CO is seeking an Open Rank Clinical Trial Coordinator (Entry – Senior) in Cardiology. This role supports interventional cardiology and imaging research, electrophysiology, and heart failure, focusing on data collection, interpretation, and documentation for multiple trials.

Responsibilities include CRF data entry, source documentation, enrollment logistics, EMR screening, consent documentation, and coordinating sponsor visits with the