Clinical Research Coordinator

This role involves coordinating clinical research within a new, technology-driven environment, focused on high-quality patient experience and data accuracy. The position requires a proactive individual capable of managing multiple tasks and learning to thrive in a fast-paced, changing research setting. They will lead patient recruitment, contribute to data integrity, and improve study efficiency and success.

Requirements

• Visit preparation activities
• Supply and inventory management
• Third-party vendor coordination
• Patient recruitment and enrollment
• Patient study visits (ECG, vitals, etc.)
• Patient consent administration
• Protocol adherence and data integrity
• Data entry and reporting
• IP management
• Data Quality and compliance
• Adverse Event management
• CoV close-out
• Quality Control