Clinical Trial Site Monitor
Company: VirtualVocations
Location: Beaumont
Posted on: October 30, 2024
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Job Description:
A company is looking for a Clinical Trial Site Monitor
(contractor, temporary, remote).
Key Responsibilities
Conduct centralized monitoring activities and ensure compliance
with regulatory standards
Provide detailed reports on site progress, findings, and concerns
based on centralized data review
Verify informed consent, data integrity, and proper reporting of
adverse events
Qualifications
Bachelor's degree in a life science, healthcare, or related
field
Substantial clinical research experience and knowledge of Good
Clinical Practice (GCP) guidelines
Certification from a recognized organization such as SOCRA or ACRP
is preferred
Prior experience in monitoring or study coordination roles
Thorough understanding of regulatory requirements and clinical
trial protocols
Keywords: VirtualVocations, Port Arthur , Clinical Trial Site Monitor, Healthcare , Beaumont, Texas
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