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As a Clinical Research Associate, you will conduct and monitor clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with site staff and investigators.

As a Senior Clinical Research Associate, you will oversee clinical trials, ensuring adherence to protocols and regulatory standards, managing multiple sites, and collaborating with teams for data integrity and compliance.

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.

Lead biostatistical components in clinical trials, oversee statistical activities, mentor junior statisticians, and ensure regulatory compliance.

Manage end-to-end contract lifecycle for clinical trial operations: draft, review, negotiate agreements, ensure regulatory compliance, advise project teams, monitor contract performance, and maintain contract records.

Conduct site qualification, monitoring, and close-out visits for clinical trials while ensuring compliance and data integrity. Collaborate with investigators and prepare study documentation.

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

The Senior Manager will oversee clinical site engagement, develop relationships with investigational sites, conduct site-level activities, and ensure compliance with protocols and regulatory requirements.

Responsible for monitoring cardiovascular medical device studies, ensuring compliance with FDA regulations, and fostering effective relationships with stakeholders.

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