Clinical Trial Quality Control Monitor

Job Summary

A company is looking for a Clinical Trial Quality Control Monitor.

Key Responsibilities

• Perform detailed quality control reviews of clinical trial documentation to ensure compliance and data accuracy
• Generate comprehensive QC reports highlighting discrepancies and documentation issues
• Serve as a subject matter expert on clinical research documentation and QA processes

Required Qualifications

• Bachelor's degree in biology, chemistry, biochemistry, physiology, nursing, or related fields
• Three or more years of experience as a Clinical Research Associate or clinical trial monitor for Oncology and/or Hematology trials
• Familiarity with Investigational New Drug procedures, study protocols, and Good Clinical Practices (GCPs)
• Trained and certified as a Clinical Research Associate or Clinical Research Professional within one year of hire