Join Providence Research as a Clinical Research Coordinator, helping to advance clinical studies through effective coordination and collaboration. This role requires expertise in multiple studies and participant management.
Reporting to the Director of Clinical Research Administration, you'll coordinate clinical trials from start-up to closeout. Your skills in regulatory compliance, participant recruitment, and data management will empower scientists and improve patient care. Your adaptability will shine as you support various Principal Investigators and study teams across Providence Research.
Key Responsibilities:
• Lead clinical research studies from start-up to closure
• Partner effectively with multiple Principal Investigators
• Manage participant recruitment and informed consent processes
• Ensure compliance with regulatory standards and best practices
• Maintain accurate study documentation and data integrity
Requirements:
• Bachelor’s Degree in health ...