Clinical Research Coordinator - Women's Health Department

Job description

If you are a current University Health or University Health Physicians employee and wish to be considered, you must apply via the internal career site. Please log into myWORKDAY to search for positions and apply. Clinical Research Coordinator - Women's Health Department 101 Truman Medical Center Job Location University Health Truman Medical Center Kansas City, Missouri Department Admin Womens Health UHTMC Position Type Full time Work Schedule 8:00AM - 4:30PM Hours Per Week 40 Job Description Responsible for performing diverse administrative and clinical responsibilities requiring some analysis, sound judgment, and a high level of knowledge of specific research study protocols, Good Clinical Practice Guidelines, Federal research regulations, and institutional requirements. Responsible for coordination and management of clinical study protocols and along with the research investigator, manages many aspects of the clinical trial and conducts all research activities within an ethically based framework in accordance with federal, state, and local regulations. Function as a liaison between investigators, subjects and sponsors, the Institution(s), Institutional Review Board (IRB) and Privacy Board. Minimum Requirements Bachelor’s degree in allied health medical field, another related field or licensed LPN. Ability to prioritize and complete several tasks/projects simultaneously in strict accordance with regulations, policies, and study protocol. Demonstrated effective verbal/written communication skills, analytical skills, attention to details, and ability to work independently with minimal supervision. Organization/time management skills and project management skills. Demonstrated intermediate knowledge of personal computer skills. Preferred Qualifications One year clinical research experience. Clinical Research Coordinator Certification (by either the Association for Clinical Research Professionals or Society of Clinical Research Associates). Knowledge of Good Clinical Practices, U.S. Department of Health and Human Services Protection of Human Subjects and U.S. Food and Drug Administration regulations, International Conference of Harmonization Guidelines, and the HIPAA Privacy Rule as it impacts clinical research