Clinical Operations: Clinical Monitoring and Site Management

To enable better performance at the investigational site, LBR provides a number of Clinical Monitoring and Site Management services.

Clinical monitoring and site management services are performed by full-time Clinical Research Associates (CRAs) who have completed training on, and are well versed in, Good Clinical Practice, Human Subjects Protection, LBR Standard Operating Procedures, and project specific processes.

When new CRAs are onboarded, their training is tooled to the individual’s experience. All employees are subject to our ongoing CRA quality control program.

LBR also maintains a list of preferred contract CRAs who meet the same quality standards as employee CRAs. LBR has a list of contract CRAs who have worked with the company for many years.

Clinical Monitoring and Site Management Services Include: