Clinical Research Monitor

Job Summary

A company is looking for a Clinical Research Monitor (Remote) to ensure the integrity and compliance of clinical trials.

Key Responsibilities

• Design and implement risk-based quality management frameworks and centralized monitoring processes
• Review study protocols for feasibility of Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs)
• Analyze clinical data to detect site performance issues and provide actionable recommendations

Qualifications

• 3+ years of experience in centralized monitoring within a CRO or clinical research setting
• Prior experience as a CRA or equivalent monitoring role
• Experience with infectious disease or oncology clinical research studies
• Strong knowledge of ICH-GCP, FDA regulations, and risk-based monitoring principles
• Bachelor's degree in life sciences or related field; advanced degree preferred