What are the responsibilities and job description for the Clinical Research Coordinator - Women's Health Department position at University Health KC?
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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
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.
- 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