Clinical Research Coordinator - Cancer Center; North Community Site

Overview

Clinical Research Coordinator - Cancer Center (North Community Site) at University of Kansas Medical Center. Located at 8700 North Green Hills Rd., Kansas City, Missouri. This role works with multidisciplinary teams to recruit, screen, educate, and coordinate clinical studies, managing data collection, documentation, and analysis, and monitoring participant progress and adverse events.

• Under the direction of the principal investigator, recruit and educate potential patients for and evaluate 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 per protocol and institutional policies.
• Ensure adequate study supplies; track study expenditures and submit reimbursement requests for equipment, supplies, and enrolled participants.
• Prepare documentation and participate in study monitoring visits, reviews, and audits; provide written and verbal reports to the PI and Project Manager as required.
• Participate in quality assurance activities by reviewing clinical data, assessing pharmacy compliance with protocol criteria, and ensuring adherence to GCP guidelines and FDA CFR.
• Collaborate with the Research Institute and Human Research Protection Program; maintain working knowledge of KUMC policies and procedures.
• Attend continuing education, research, and training seminars as requested by the manager.

• 4 years of relevant work experience. Education may be substituted on a year-for-year basis.
• Experience with regulations governing clinical research (CFR, GCP, HIPAA).
• Experience with regulatory affairs in clinical research, including study budgets, contracts, and grant applications.

• Bachelor’s degree.
• Certifications/Licenses:
  Certified Clinical Research Coordinator (CCRC);
  Certified Clinical Research Professional (CCRP).

• Communication
• Organization
• Multi-tasking

This position will be 100% onsite as it is a patient-facing role.

Comprehensive benefits begin on day one, including health, dental, and vision insurance, life insurance, long-term disability, and various voluntary insurance plans. Paid time off accrues from hire, with holidays, discretionary days after six months, and leave for bereavement, jury duty, military service, and parental leave after 12 months. Retirement programs (457/403b) with employer contributions are available. Pay range: $58,656.00 - $86,000.00;

minimum $58,656.00; midpoint $72,328.00; maximum $86,000.00.

Required documents:
Resume, Cover Letter.