Clinical Research Coordinator

About This Role

This role involves managing a portfolio of surgical clinical trials for the Department of Cardiac Surgery, focusing on advancing healthcare outcomes for patients. The Clinical Research Coordinator will apply critical thinking and problem-solving skills across various clinical studies.

Responsibilities

• Perform study procedures with accuracy
• Triage complex study concerns appropriately
• Schedule, prepare for, and attend study initiation meetings, monitor visits, and audits
• Manage increasing levels of protocol complexity and/or volume efficiently
• Lead aortic clinical trials under supervision of Clinical Trial Lead and Clinical Research Manager
• Contribute to the development of processes and tools to capture data in accordance with ALCOA-C principles
• Create CRFs, study documents, and tools
• Resolve complicated queries
• Monitor site compliance with subject safety reporting, escalate issues, and contribute to the development of tools and processes to enhance subject safety
• Provide logistic and regulation guidance on Investigator Initiated Studies for adherence to University and Federal guidelines
• Oversee aortic clinical research coordinators
• Support study team members on a range of communication and teamwork best practices
• Participate in trainings specifically for maintaining certification as a Clinical Research Professional

Requirements

• Bachelor's degree in Health Science or equivalent
• Certification (CCRC or CCRP) required within six months of hire
• Minimum 3 years of clinical research and clinical trials experience

Qualifications

• Bachelor's degree in Health Science or an equivalent combination of related education and experience
• Minimum 3 years of directly related experience in clinical research and clinical trials

Certifications