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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.

As a Clinical Research Associate, you will monitor clinical trials, ensuring adherence to protocols and regulations, conduct site visits, and train staff.

The manager will oversee operational planning, implement process improvements, manage KPIs, and coach team members to enhance efficiency.

Oversee and manage clinical trial activities, ensuring compliance with protocols and regulations, while mentoring 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 sites; review data and support study documentation.