Clinical Research Coordinator - 119425

Overview:Contract (Expected to go though the end of the year)Full-time M-F (Standard business hours)Medical Device StudyPOSITION SUMMARY:The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager, the Principal Investigator and the Medical Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols.Duties and Responsibilities:Administratively and clinically manage an average of six to eight clinical trialsAdhere to Research SOP'sAdhere to Good Clinical Practices and the study protocolsEnsure scientific integrity of data and protect the rights, safety, and well-being of patientsenrolled in clinical trialsDiscuss study protocols with patients and verify the informed consent documentationProvide patient with written communication of their participation (i.e. copy of the signedinformed consent)Dispense study medication in a professional and accountable manner following protocolrequirementsPerform ECGs and obtain vital signs of patientsSchedule all patient research visits and procedures consistent with protocolrequirements

Created: 2025-03-03