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Clinical Research Coordinator

Medix

Participant Management: Recruits, screens, and enrolls eligible patients; obtains informed consent; and coordinates study visits. Data and Record Keeping: Collects patient data, records vital signs, processes lab specimens, and enters information into case report forms or databases. Regulatory Compliance: Ensures the study follows Good Clinical Practice (GCP) guidelines, FDA regulations, and Institutional Review Board (IRB) rules. Safety Monitoring: Tracks and reports adverse events or side effects experienced by participants. Communication: Acts as the primary point of contact for patients, answers sponsor queries, and liaises with laboratories #J-18808-Ljbffr

Vacancy posted 1 day ago
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