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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.

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

The Clinical Research Associate will conduct site visits, ensure protocol compliance, review data, and collaborate with investigators to facilitate clinical trials.

As a Global Study Manager, you will oversee clinical budgets, develop monitoring plans, manage study start-ups, drive enrollment, and foster relationships with stakeholders.

As Global Study Lead, you will manage clinical trial aspects, focusing on budget oversight, study monitoring, enrollment, and stakeholder relations.

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

Oversee and monitor clinical trial sites to ensure protocol, regulatory and GCP compliance; conduct site visits; manage multiple sites; ensure data integrity and participant safety; train and support site staff; collaborate with cross-functional teams and maintain stakeholder relationships.

As a Clinical Research Associate, you will oversee clinical trial activities, ensuring compliance with protocols and regulations, and provide support to trials.

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

The Feasibility Principal Analyst leads feasibility strategy and analysis for clinical studies, synthesizing data to inform study planning and enrollment decisions while mentoring junior team members.