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If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet, please review this tip sheet. The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Clinical Research Coordinator 1 to work at the UHealth Medical Campus in Miami, FL 33146. CORE JOB SUMMARY The Clinical Research Coordinator 1 serves as an entry level clinical research professional that has a basic foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. This role exhibits increased learned skills and flexibility in performing duties and assumes responsibility for simple clinical research protocols and timelines. CORE JOB FUNCTIONS 1. Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols. Maintains enrollment procedures according to the protocol. 2. Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation. 3. Performs moderate to complex research tests/ experiments and adapts procedures for quality improvement under supervision. 4. Understands and follows technical instructions for operating clinical research equipment, problem solves when operational failures occur. 5. Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants. 6. Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study. 7. Identifies, reports, and helps problem solve protocol deviations and unanticipated occurrences. 8. Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies. 9. Knows the contents and maintenance of study-specific clinical research regulatory binders. 10. Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies. 11. 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. CORE QUALIFICATIONS Education: Bachelor's degree in relevant field required Experience: Minimum 1 year of relevant experience Knowledge, Skills and Attitudes:...opportunity to build dream vacations and business travel with major vendors such as Expedia,... ...Cruises, Sandals, Delta and many more Online! Arrange Travel for businesses... ...Protection ~ Daily Training Available ~ Travel Agent Certification...
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