Clinical Trial Site Monitor

Job Summary

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