Manages a team in the Clinical Network with a focus on performance oversight, regulatory compliance, training, resource allocation, and client relationships.

The Clinical Research Associate I monitors and manages clinical study sites, ensuring regulatory compliance, data integrity, and effective communication with stakeholders.

As a Clinical Research Associate II, you will manage and monitor clinical trials, ensuring compliance with regulations and building relationships with investigative sites. Responsibilities include site monitoring, data integrity checks, and preparing project plans. Occasional travel is required for site visits.