Clinical Trial QC Monitor

Job Summary

A company is looking for a Clinical Trial QC Monitor.

Key Responsibilities

• Performs comprehensive quality control monitoring of source documentation for clinical trials
• Generates QC reports summarizing deviations, discrepancies, and missing documentation
• Conducts QC monitoring, investigates protocol deviations, and provides training to relevant personnel

Required Qualifications

• Bachelor's degree in a scientific field such as biology, chemistry, or nursing
• Minimum of three years of experience as a Clinical Research Associate or clinical trial monitor, preferably in Oncology and/or Hematology
• Strong understanding of IND procedures, study protocols, and regulatory requirements
• Knowledge of Good Clinical Practice (GCP) guidelines and clinical research standards
• Must obtain certification as a Clinical Research Associate (ACRP) or Clinical Research Professional (SoCRA) within one year of hire