Clinical Research Coordinator

Key Responsibilities

• Oversee daily clinical site operations across multiple therapeutic areas
• Drive patient recruitment, screening, and enrollment performance
• Ensure compliance with FDA, GCP, and protocol guidelines
• Manage, mentor, and develop site staff (clinical and administrative)
• Monitor KPIs: enrollment, retention, data quality, and operational efficiency
• Collaborate with Sponsors, CROs, and internal leadership
• Optimize workflows and enhance patient experience
• Identify and resolve operational bottlenecks
• Ensure high-quality execution across all clinical trials

Qualifications

• 5+ years of clinical research experience, including site management
• Experience in CNS / psychiatric clinical trials
• Strong understanding of GCP, FDA regulations, and trial operations
• Proven ability to improve enrollment and site performance
• Experience managing cross-functional teams
• Strong leadership, organizational, and communication skills