Maryland Licensed Clinical Research Monitor

Job Summary

A company is looking for a Clinical Research Monitor who will lead compliance monitoring of clinical trials.

Key Responsibilities

• Manage site and study progress by tracking regulatory submissions and data query resolution
• Conduct risk assessments and develop monitoring plans based on findings
• Ensure compliance with regulatory requirements and assist in training research staff

Required Qualifications

• Bachelor's Degree in a related field
• Minimum 5 years of experience with clinical trials or medical research
• Thorough knowledge of ICH GCP and FDA guidelines
• Experience using Electronic Data Capturing (EDC) systems
• Additional education may substitute for required experience as permitted by the equivalency formula