University Health
The Clinical Research Coordinator manages clinical study protocols and ensures all research activities comply with federal, state, and institutional regulations. They act as a liaison between investigators, research subjects, sponsors, and the Institutional Review Board.
Candidates must hold a bachelor's degree in an allied health or related field, or be a licensed LPN. Strong analytical, organizational, and communication skills are required, with a preference for one year of clinical research experience and relevant professional certification.
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
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.
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 Working at University Health is about making a difference. It's providing the best care to every patient every day. University Health (UH), is committed to being a leader in providing a culturally inclusive workplace for our employees. UH is an equal opportunity employer. We value and celebrate our differences. We are committed to equal employment opportunity regardless, but not limited to race, ethnicity, religion, beliefs, sex (including pregnancy, gender identity and expression, sexual orientation), national origin, ancestry, language, age, citizenship, genetic information, marital status, socioeconomic status, literacy, disability, mobility, abilities, veteran status and any other category protected by applicable law.
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