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This role involves overseeing clinical trials for cardiovascular/electrophysiology medical devices, ensuring regulatory compliance, and managing site relationships.

The Clinical Trial Assistant will support clinical trials through administrative tasks, documentation management, and stakeholder communication to ensure smooth operations and compliance with regulations.

The Clinical Research Associate II role involves coordinating clinical trials, ensuring compliance, collaborating with site staff, and maintaining data integrity.

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; review data and resolve queries; contribute to study documentation and reporting.

The Clinical Research Associate manages clinical trial site activation by conducting site qualification visits, ensuring compliance with regulations, and collaborating with study teams and site staff to achieve study timelines.

The Senior Clinical Research Associate will manage clinical trials by conducting site visits, ensuring compliance, and contributing to study documentation.

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with sites; review data and support study documentation.