As a Clinical Research Associate I, you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation
Job Summary
As a Clinical Research Associate I, you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.).
You will ensure audit readiness and develop collaborative relationships with investigational sites.
Matching Summary
As a Clinical Research Associate I, you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
Skills & Requirements
Must-have
Risk-based monitoring approach
ICH-GCP guidelines
Site processes specialist
Investigational product assessment
Essential documents completion
Nice-to-have
Collaborative relationships with sites
Contribute to project publications
Process improvement initiatives
Key Requirements
Bachelor's degree in life sciences or RN certification