Research Coordinator I/II/III

at  Cleveland Clinic

Research Coordinator II
Taussig Cancer Center is the hub for Cleveland Clinic Cancer Center. With locations throughout Northern Ohio and in Weston, Florida, Cleveland Clinic Cancer Center provides comprehensive care for patients with cancer. Our multidisciplinary cancer programs are designed to streamline care and improve patient outcomes. Cleveland Clinic Cancer Center provides a range of services to patients including clinical trials and internationally-recognized cancer research efforts ensuring patients have access to the latest advances in cancer treatment, as well as a range of support programs helping patients navigate the challenges associated with a cancer diagnosis. Cleveland Clinic is recognized in the U.S. and throughout the world for its expertise and care.
Innovative research and groundbreaking discoveries happen every day at
Cleveland Clinic. Each member of our team contributes to our mission of caring for life, researching health and educating those who serve. We’re creating an environment of belonging—where everyone is valued and respected—dedicated to collaboration, mentorship, diversity and inclusion.

PHYSICAL REQUIREMENTS:

• Ability to perform work in a stationary position for extended periods
• Ability to operate a computer and other office equipment
• Ability to communicate and exchange accurate information
• In some locations, ability to move up to 25 pounds

• Coordinate the compliant implementation and conduct of human subject research projects, typically of medium workload and medium complexity.
• Maintain regulatory documents and binders, conduct data management, complete IRB submissions and communicate with the research team.
• Report and complete serious adverse events and/or safety logs.
• Communicate with sponsors, monitors and research personnel to ensure all aspects of study compliance.
• Serve as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions.
• Schedule pre-site selection visits, site initiation visits, webinars, monitoring and close-out visits.
• Plan, conduct and evaluate project protocols and research subject recruitment.
• Monitor and report project status and research data.
• Complete regulatory documents, data capture, monitoring plans and protocol-related activities.
• Assist with preparing and responding to audits and maintaining research tools