Performs and coordinates all aspects of the clinical monitoring and site management process, ensuring subjects' rights, well-being, and data reliability
Job Summary
Performs and coordinates all aspects of the clinical monitoring and site management process, ensuring subjects' rights, well-being, and data reliability.
Monitors investigator sites with a risk-based monitoring approach, applying root cause analysis and critical thinking to identify and resolve site process failures.
Offers a comprehensive Total Rewards package including medical, dental, vision plans, retirement savings, and paid time off.
Matching Summary
Performs and coordinates all aspects of the clinical monitoring and site management process, ensuring subjects' rights, well-being, and data reliability.
Salary
Base: $66,800.00–$112,938.00; Bonus/Equity: Variable annual bonus based on performance; Benefits: Comprehensive Total Rewards package
Skills & Requirements
Must-have
Risk-based monitoring approach
ICH-GCP guidelines
Site processes specialist
Investigational sites collaboration
Protocol and regulatory compliance
Nice-to-have
Oncology, HIV, respiratory experience
Effective interpersonal skills
Adaptable in wide range of scenarios
Key Requirements
1+ years as a clinical research monitor
Bachelor's degree or equivalent
Valid driver's license
Legally authorized to work in the US without sponsorship
Work Rights
Must be legally authorized to work in the United States without sponsorship