Hybrid Cancer Clinical Research Coordinator

University of Colorado Anschutz; Aurora (CO); Hybrid; USD 55,000 - 75,000; Full time

Job summary

University of Colorado Anschutz Medical Campus is seeking a Clinical Research Coordinator to support cancer center studies. The role covers patient-oriented and data-driven research activities within a collaborative team environment.

You will participate in consent processes, data collection, and coordination of study visits, with an emphasis on regulatory compliance and high-quality data capture. The Hybrid schedule becomes fully on-site as needed by trials.

Qualifications

• Bachelor's degree in any field required or equivalent experience.
• Bachelor's degree in science or health-related field preferred.

Responsibilities

• Understand workflows and requirements for studies at UCHealth and Rocky Mountain Regional VA Medical Center.
• Oversee day-to-day operations of cancer prevention and survivorship research studies and clinical trials.
• Abstract and record subject data onto CRFs and into clinical trials database accurately and timely.
• Assess eligibility by reviewing medical history and current medications for trial participation.
• Obtain informed consent and ensure proper documentation and filing of consent forms.
• Recruit prospective subjects through interviews and calls, explaining study details.

Skills

GCP knowledge

Excellent communication

Team collaboration

Patient interaction

Data entry accuracy

Education

Bachelor's degree in science or health-related field

Tools

EMR/EHR data management systems

Clinical trial documentation

Job description

University of Colorado Anschutz Medical Campus is seeking a Clinical Research Coordinator to support cancer center studies. The role covers patient-oriented and data-driven research activities within a collaborative team environment.

You will participate in consent processes, data collection, and coordination of study visits, with an emphasis on regulatory compliance and high-quality data capture. The Hybrid schedule becomes fully on-site as needed by trials.