University of Pennsylvania Perelman School of Medicine

Clinical Research

• Manage phases of complex clinical trials under general supervision
• Ensure compliance with good clinical practice
• Coordinate with partnering institutions
• Support monitoring of external sites
• Participate in study and protocol training meetings
• Assist with participant recruitment and enrollment
• Support data collection and management
• Maintain study documentation
• Ensure adherence to study protocols and regulatory requirements
• Communicate with study participants
• Track study progress
• Prepare study materials and reports
• Supervise study research assistants
• Provide day-to-day oversight for accurate study activity conduct
• Lead study-related meetings
• Assist with IRB submissions and updates
• Support data quality assurance processes
• Contribute to study reporting and manuscript preparation

Clinical Research Coordinator