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Clinical Trial Site Monitor

Company: VirtualVocations
Location: Beaumont
Posted on: October 30, 2024

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, Texas City , Clinical Trial Site Monitor, Healthcare , Beaumont, Texas

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