Job Details

A company is looking for a Senior Clinical Research Monitor (Remote).Key ResponsibilitiesPerform ongoing internal reviews of regulatory documents and protocol compliance for IRB approved trialsConduct Exit Conferences with Investigators and assist in regulatory agency inspections and auditsDevelop educational materials and recommend changes in policies to ensure compliance with regulationsRequired QualificationsBachelor's Degree in a Science related field; Master's Degree preferred7+ years of experience as a clinical research coordinator, including at least 5 years of auditing/monitoring experienceACRP Certification strongly preferred