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Clinical Trial Site Monitor

VirtualVocations
Fort Lauderdale, Florida, United States
Full-time

A company is looking for a Clinical Trial Site Monitor (contractor, temporary, remote).Key ResponsibilitiesConduct centralized monitoring activities and ensure compliance with regulatory standardsProvide detailed reports on site progress, findings, and concerns based on centralized data reviewVerify informed consent, data integrity, and proper reporting of adverse eventsQualificationsBachelor's degree in a life science, healthcare, or related fieldSubstantial clinical research experience and knowledge of Good Clinical Practice (GCP) guidelinesCertification from a recognized organization such as SOCRA or ACRP is preferredPrior experience in monitoring or study coordination rolesThorough understanding of regulatory requirements and clinical trial protocols

15 hours ago
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