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Coordinates routine activities of clinical studies including data maintenance, grant expenditure adherence, project evaluation, meeting scheduling, and research subject interfacing. Tracks medical reports and reviews regulatory documents to generate reports. Serves as project liaison to other departments, outside organizations, government agencies, and product representatives. Engage with stakeholders in the African-American community to develop state-of-the art research programs that will serve older adults. Recruits patients into the study and reviews on a weekly basis the percentage recruited. Reviews data collected and inserts into the study dataset. Compares the data collected to the monitored phone calls for data quality assurance. Evaluates and monitors timelines for studies and for each subject participant to comply with applicable protocols. Prepares materials for the brochures and retaining letters and mails to appropriate members according to their time in the study. Administers informed consent forms for patients on drug studies. Maintains pool of study candidates and ensures their availability. Coordinates the necessary testing for patient evaluations per physicians' orders and study protocol requirements. Adheres to University and unit-level policies and procedures and safeguards University assets.
This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.
Bachelor's Degree in relevant field required
Certification and Licensing:
Minimum 3 years of relevant experience
Knowledge, Skills and Attitudes: