Clinical Research Coordinator 248103
MedixWest Jordan, UT, United StatesHace 1 día
Tipo de contrato
- A tiempo completo
Descripción del trabajoTrial management : Coordinate all aspects of clinical trials, from startup to closeout, ensuring adherence to protocols and timelines. Participant management : Recruit, screen, and enroll eligible participants; obtain informed consent; and monitor participant safety and compliance throughout the study. Data management : Collect, enter, and validate clinical trial data, ensuring accuracy and completeness. Generate reports and maintain study-related documentation, including case report forms and other regulatory forms. Regulatory compliance : Ensure all trial activities comply with relevant regulations, Good Clinical Practice (GCP), and ethical guidelines. Prepare and submit documents to the Institutional Review Board (IRB). Liaison and communication : Act as a point of contact for investigators, sponsors, laboratories, and regulatory bodies.
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Clinical Research Coordinator • West Jordan, UT, United States
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