Cardiology Clinical Trial Coordinator (Open Rank) - Onsite

University of Colorado Anschutz

Aurora (CO)

On-site

USD 50,000 - 72,000

Full time

3 days ago
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Job summary

University of Colorado Anschutz Medical Campus is seeking a Clinical Trial Coordinator for cardiology-related interventional and imaging research. The role focuses on data collection, interpretation, and documentation of clinical research data, with onsite duties in Aurora, CO.

Responsibilities include managing CRFs, reviewing EMRs, coordinating prescreening and enrollment, and assisting with sponsor monitors and audits in collaboration with the regulatory team and CRC.

Qualifications

  • Bachelor's degree in any field.
  • 1 year of clinical research or related experience.
  • Ability to work onsite in Aurora, CO.

Responsibilities

  • Abstract and record patient data on CRFs and in the Clinical Trials database.
  • Ensure complete source documentation is compiled in research records.
  • Schedule and track prescreening, screening and enrollment logs.
  • Obtain and review electronic medical records via EPIC for identifying and screening potential subjects.
  • Gather and maintain source documents, regulatory binders, and subject binders.
  • Ensure current consent forms are completed and documented.
  • Review medical history to determine eligibility.
  • Schedule, coordinate, prepare for and conduct sponsor monitor visits and audits with the regulatory team and CRC.

Skills

GCP knowledge
Effective communicator
Team collaboration
Research ethics

Education

Bachelor's degree

Tools

EPIC
Oncore
REDCap

Job description

University of Colorado Anschutz Medical Campus is seeking a Clinical Trial Coordinator for cardiology-related interventional and imaging research. The role focuses on data collection, interpretation, and documentation of clinical research data, with onsite duties in Aurora, CO.

Responsibilities include managing CRFs, reviewing EMRs, coordinating prescreening and enrollment, and assisting with sponsor monitors and audits in collaboration with the regulatory team and CRC.

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