Clinical Research Monitor

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