Senior Clinical Research Monitor

Location: Remote
Compensation: To Be Discussed
Reviewed: Tue, Apr 14, 2026
This job expires in: 13 days

Job Summary

A company is looking for a Senior Clinical Research Monitor (Remote).

Key Responsibilities
  • Perform ongoing internal reviews of regulatory documents and protocol compliance for IRB approved trials
  • Conduct Exit Conferences with Investigators and assist in regulatory agency inspections and audits
  • Develop educational materials and recommend changes in policies to ensure compliance with regulations
Required Qualifications
  • Bachelor's Degree in a Science related field; Master's Degree preferred
  • 7+ years of experience as a clinical research coordinator, including at least 5 years of auditing/monitoring experience
  • ACRP Certification strongly preferred

COMPLETE JOB DESCRIPTION

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