Clinical Research Associate.UHC Peds Pulmonary-50730
- Location: Cleveland, OH
- Posted: Sep 6, 2019
Assists in the conduct of clinical research projects/studies involving various modalities of treatment for gastroenterology patients in compliance with the approved protocol and the regulations of all internal and external regulatory agencies. Essential duties include: Recruit, screens and enrolls patients for potential research study participation. Monitors subjects adherence to protocols to maintain protocol compliance. Documents, records and assimilates accurate, patient records and study records to insure documentation compliance with sponsor guideline and internal and external regulatory agencies. Performs required testing and procedures for individual study protocols. Participates in the development and initiation of new projects. Liaison with study sponsors. Prepares and condenses protocols for the approval of the IRB new project. Assist with budgetary preparation for investigational studies. Involved in learning and self-improvement.
Requires the academic knowledge in a health science or social science discipline, that is generally associated with a Bachelor’s degree, supplemented by one or more years of progressively responsible experience in the conduct of clinical research or the equivalent combination of health or social science education and experience.
Minimum 2 years of progressive clinical experience in a health related field and 1 year of experience in the regulatory aspects of medical research and procedures in the conduct of clinical trials.