About This Opportunity
Lead clinical trials for Puzzle Medical as a Clinical Program Manager, ensuring timely execution and compliance for Class II and III medical devices. This role requires expertise in site management and hands-on monitoring.
As the Clinical Program Manager, you'll oversee the operational execution of clinical trials, guiding studies from Early Feasibility to pivotal phases. Your responsibilities will encompass site selection, activation, and performance management, coupled with CRA and CRO oversight for later-stage studies. The role demands strong leadership skills and a deep understanding of regulatory compliance and best practices.
Key Responsibilities:
• Manage clinical studies from initiation through close-out
• Conduct monitoring for Early Feasibility Studies (EFS)
• Build infrastructure for pivotal trials and manage CRAs
• Optimize site activation timelines and manage compliance
• Implement risk-based monitoring strategies
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