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Clinical Research Coordinator
Position Description: Clinical research coordinator to assist with all aspects of research including protocol review, site preparation, informed consent, subject recruitment, data collection and completion of CRFs, follow-up visits, reporting of AEs and SAEs, deviations, and queries.  Maintains regulatory binders.  Assists the PI in the consent process, screening, scheduled visits.  Must be current on Good Clinic Practice, protection of human subjects in research practices, and FDA regulatory guidelines regarding clinical research. Essential Responsibilities: Assist the PI in all aspects of conducting the clinical study following the FDA and Sponsor regulations and guidelines. Ensures the safety and welfare of


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