Clinical Research Assistant - Cancer Center

Coordinate clinical research activities for cancer trials: recruit, evaluate, and educate patients regarding clinical trials; conduct informed consent interviews; document trial-related activities per regulatory requirements; coordinate participant visit scheduling and procedures; maintain regulatory documentation with sponsor, IRB, and subjects; provide written/verbal reports to Principal Investigator and Project Manager. Must have strong attention to detail, time management, interpersonal, and computer skills (experience with electronic medical records, data management, and tools like REDCap, Excel, Access). Role is 100% onsite in the Kansas City metro area. Education: Bachelor’s degree in a relevant field preferred; 2 years of related work experience required; ability to substitute education on a year-for-year basis.