Clinical Research

• Handle administrative activities generally associated with the conduct of clinical trials
• Provide guidance to less experienced staff
• Manage research project databases
• Develop flow sheets and other study-related documents
• Complete source documents and case report forms
• Interface with research participants
• Determine eligibility and consent study participants according to protocol
• Approve orders for supplies and equipment maintenance
• Assist in developing recruitment strategies
• Conduct screenings, interviews, and questionnaires for study participants
• Supervise collection and processing of study specimens
• Establish case packages for study procedures
• Monitor scheduling of procedures and charges
• Coordinate other services as needed
• Ensure compliance with research protocols
• Review case report forms and audit accuracy against source documents
• Attend monitoring meetings with sponsors
• Prepare regulatory submissions with appropriate credentialing and training
• May perform phlebotomy or diagnostics
• Perform related approved responsibilities as required

Explore Clinical Research Coordinator II at Emory University. Review requirements and application details.

Clinical Research jobs in Georgia

Clinical Research Coordinator II

Supervisor, Clinical Research Data Team

Clinical Research Coordinator II