CLINICAL RESEARCH COORDINATOR: Coordinates and manages all components required for an organized multi-disciplinary team approach for the successful participation and completion of clinical research trials in TriHealth. Functioning as an educator, consultant/liaison, and evaluator, the Clinical Research Coordinator strives to coordinate clinical research trials with safety, integrity and efficiency while applying knowledge of good clinical practices. Coordinates Phase II thru IV trials from initial sponsor contact for site selection, study preparation and execution to study completion and close-out. Responsible for marketing and networking with sponsors. Determines protocol feasibility and some budgetary issues. Adheres to the standard operating procedures of the TriHealth Hatton Research Institute.
DEPARTMENT SPECIFICS: Preferred oncology research experience, preferred Oncology Nurse Certification (ONC), must be detailed oriented, able to multi-task, and willing to travel to satellite sites
MINIMUM REQUIREMENTS: EDUCATION: Bachelor's Degree in Biological Science Hard Sciences, Psychology, Sociology BLS/CPR (Basic Life Support for Healthcare Providers) Certified Clinical Research Coordinator (Within 2 years for Full-time and within 4 years for Part-time positions EXPERIENCE: None SPECIALIZED KNOWLEDGE: None
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