The Clinical Research Coordinator 1 serves as an entry-level clinical research professional with foundational clinical research responsibilities including data management and implementing clinical research protocols. Duties include performing chart review/pre-screening for study participant eligibility, coordinating simple clinical research protocols, maintaining enrollment procedures, scheduling study visits and appointments, performing moderate to complex research tests/experiments, operating clinical research equipment, reporting adverse events, addressing protocol deviations, and adhering to regulatory requirements. The role requires maintaining study-specific regulatory binders, mandatory training, and compliance with University policies. Department-specific functions include establishing patient screening procedures, handling multiple clinical trials, obtaining informed consent, recruiting patients, processing biological samples, collaborating with research pharmacy, completing audit corrections, maintaining contact with stakeholders, updating agencies, providing education on protocols, entering data into electronic systems, maintaining regulatory and participant files, submitting IRB continuing reviews and amendments, implementing protocols, invoicing sponsors, and traveling to investigator meetings and Bascom Palmer Eye Institute sites as needed. The position requires a Bachelor’s degree in a relevant field and a minimum of 1 year of relevant experience. Skills include attention to detail, ability to prioritize work under pressure, discretion with confidential information, flexibility to work evenings/nights/weekends, and ability to work independently or collaboratively. The University of Miami offers competitive salaries and comprehensive benefits.
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