Research Coordinator

• Responsible for data management for phase I, II, and III oncology clinical trials
• Support all aspects of clinical research data management for clinical trials
• Collect data from source documents and medical records
• Complete case report forms per sponsor requirements
• Review and analyze information from medical records to extract data
• Accurately capture data in electronic or paper Case Report Forms
• Ensure query resolution with proper physician and clinical study team oversight
• Request and upload radiological images into sponsor-provided imaging platforms
• Collect and organize source documents in electronic and paper format
• Ensure accuracy of data entered in the Clinical Trials Management System
• Interface with study team members to resolve discrepancies
• Schedule sponsor monitoring and study close-out visits
• Provide support during internal and external monitoring and auditing preparation
• Communicate with pharmaceutical sponsors, study monitors, auditors, physicians, and study team members
• Collaborate closely with physicians and Study Coordinators to maintain protocol integrity
• Assist with training of incoming Research Data Coordinators

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Research Data Coordinator