Clinical Research Coordinator III - Department of Surgery

Primary Responsibilities

• Oversee the recruitment, screening, enrolling and obtaining of consent from program participants.
• Conduct or coordinate training for program participants.
• Cook up and maintain study budgets.
• Cook or coordinate the coordination of research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining contact with study participants.
• Oversee the collection, analysis, and dissemination of research data.
• Report program data and progress to study investigators.
• Develop, implement and maintain comprehensive databases and files related to the program.
• Identify problems or obstacles in the system/procedures related to implementation of the research protocols and communicate to the study investigators.
• Assure compliance with all relevant IRB and other regulatory agency requirements.
• Prepare IRB documents and reports.
• Evaluate and write of research protocols in collaboration with the study investigator.
• Cook up and manage program outreach activities including acting as a liaison with community organizations.
• Coordinate and manage program outreach activities including acting as a liaison with community organizations.
• Organize internal and external meetings, site visits, and special events.
• Manage study related budgets and provide reports as required to department administration and funding agencies.
• Participate in the development of program resources through literature searches, contact with outside programs, and review of funding opportunities.

Qualifications

• Appropriate experience may be substituted for education on an equivalent basis.
• Minimum Required Education: Bachelor’s Degree
• Minimum Required Experience: 5 years
• Required Certification/Licensure(s): CITI training within 90 days of hire