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The Senior Clinical Research Associate manages monitoring for cardiovascular clinical trials, ensuring compliance with FDA regulations and guiding teams to resolve site issues effectively.

As a Clinical Research Associate II, you will monitor late phase studies, ensure protocol compliance, collaborate with site staff, and conduct trial visits.

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.

The Senior Clinical Research Associate will monitor cardiovascular devices, ensuring compliance with FDA regulations and managing study communication, while travelling regionally up to 65%.

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

Perform site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance, data integrity, and patient safety. Collaborate with site staff, review data and resolve queries, and contribute to study documentation and clinical study reports.

As a Clinical Research Associate, you will conduct clinical trial monitoring, ensure protocol compliance, analyze data, and collaborate with site staff.