Under the supervision of the Clinical Site Coordinator, the Research Nurse will screen prospective participant’s study eligibility, obtain informed consents, coordinate study visit evaluations and procedures, administer vaccination or infusion therapy, complete case report forms, monitor and file adverse event reports related to study participation in COVID related grant funded research and HIV Prevention Trials Network research. S/he will participate in developing a quality management plan and oversee the site’s pharmacy coordination process with the study’s main research pharmacy. S/he will also be responsible for the collection, documentation, storing, and reporting of study data from participants in compliance with the study protocol and study specific procedures.
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