Central Monitor

Job Summary

A company is looking for a Central Monitor to drive risk-based quality management and centralized monitoring strategies for clinical trials.

Key Responsibilities

• Develop and manage risk-based quality management and centralized monitoring processes for clinical trials
• Review clinical study data, identify site performance issues, and recommend actions to CRAs
• Serve as a Subject Matter Expert (SME) during dashboard development, advising clients on best practices

Qualifications

• Thorough knowledge of ICH GCP and regulatory requirements for clinical trials
• Minimum 3 years of experience in central monitoring within a CRO setting
• Prior experience as a CRA conducting on-site monitoring or equivalent skillset
• Strong understanding of central monitoring database technologies and processes
• Experience mentoring teams and advising on best practices