Hiring: Clinical Research Coordinator - Cancer Center Company: University of Kansas Medical Center Location: Kansas City, KS Job Posted Time: 2026-09-13 11:10:21 Employment Type: Full-time Target Skills & Keywords : GCP, HIPAA, HTML, Microsoft Office, Project Management, Quality Assurance About the job Experience: •4 years of relevant work experience. Education may be substituted for experience on a year for year basis. •Certified Clinical Research Coordinator (CCRC) •Certified Clinical Research Professional (CCRP) Required Skills: •Under the direction of the principal investigator, recruit and educate potential patients for and evaluate potential patient eligibility for clinical trials. •Maintain source documents and submit case report forms (CRFs) as required for clinical trials. •Recognize and report adverse events/serious adverse events to the Principal Investigator, FDA, and sponsors. •Perform study procedures, as outlined in the protocol and within state and institutional scope of practice. •Assist clinical staff with phlebotomy and sample collection, processing, handling, and shipping as outlined in the protocol and within institutional/KUMC policy. •Ensure adequate study supplies are being maintained. Track study expenditures and submit reimbursement requests for study equipment, supplies and study participants. •Prepare documentation and participate in study monitoring visits, reviews and audits. Provide written and verbal reports to Principal Investigator and Project Manager, as required. •Participate in quality assurance activities by reviewing clinical data in medical record charts, assessing pharmacy compliance with protocol criteria and reviewing study documentation to ensure compliance with GCP guidelines and FDA CFR. Qualifications: •Bachelor’s degree. Compensation: •$60,800 - $91,200 / year Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!