Performs and coordinates all aspects of the clinical monitoring and site management process, ensuring protocol and regulatory compliance
Job Summary
Performs and coordinates all aspects of the clinical monitoring and site management process, ensuring protocol and regulatory compliance.
Monitors investigator sites using a risk-based approach, applying root cause analysis and problem-solving skills to ensure compliance and decrease risks.
Develops collaborative relationships with investigational sites and facilitates effective communication between sites, clients, and the project team.
Matching Summary
Performs and coordinates all aspects of the clinical monitoring and site management process, ensuring protocol and regulatory compliance.
Skills & Requirements
Must-have
Risk-based monitoring approach
ICH-GCP guidelines
Site process compliance
Data accuracy and reliability
Investigational product assessment
Essential document completion
Nice-to-have
Oncology experience
Collaborative relationships with sites
Process improvement contributions
Key Requirements
1+ years as a clinical research monitor
Bachelor's degree in life related field or RN certification