The Christ Hospital Health Network
Location
Cincinnati, Ohio
The Clinical Research Coordinator supports the Principal Investigator by coordinating daily clinical trial activities and ensuring data integrity. They provide guidance on compliance, financial, and personnel aspects of the study to ensure human subject safety.
A Bachelor's degree is required, with a Master's preferred, along with 2-4 years of clinical research experience. Proficiency with medical equipment, software, and strong organizational skills are essential.
Specialized research professional working with and under the direction of the Principal Investigator (PI) and the Lindner Center for Research and Education. While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. The CRC ensures quality, human subject safety and data integrity of the clinical trial. By performing these duties, the CRC works with the PI, department, sponsor, Lindner Center and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.
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