Research Coordinator I - Heart, Vascular & Thoracic Institute
Cleveland ClinicAbout the role
At Cleveland Clinic Health System, we believe in a better future for healthcare. And each of us is responsible for honoring our commitment to excellence, pushing the boundaries and transforming the patient experience, every day.
We all have the power to help, heal and change lives — beginning with our own. That’s the power of the Cleveland Clinic Health System team, and The Power of Every One.
Job Title
Research Coordinator I - Heart, Vascular & Thoracic Institute
Location
Cleveland
Facility
Cleveland Clinic Main Campus
Department
HVTI Research and Registries-Heart Vascular & Thoracic Institute
Job Code
D99967
Shift
Days
Schedule
8:00am-4:30am
Job Summary
Job Details
Join the Cleveland Clinic team where you will work alongside passionate caregivers and make a lasting, meaningful impact on patient care. Here, you will receive endless support and appreciation while building a rewarding career with one of the most respected healthcare organizations in the world.
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. As Research Coordinator I at the Heart, Vascular and Thoracic Institute, you are critical in the search for developing innovative treatments for cardiovascular illnesses. You will collaborate with a diverse team to recruit patients for clinical research studies. Some of these studies are for patients who have no other treatment option or are still suffering. There is a great need for every research study to help these patients get the care they need and deserve. You also have the unparalleled opportunity to contribute to published studies, allowing you to begin a portfolio of completed projects with a respected healthcare system. Come be part of something amazing at Cleveland Clinic and enhance patient care along the way.
A caregiver in this position works days from 8:00AM – 4:30PM.
A caregiver who excels in this role will:
Assist with coordinating the compliant implementation and conduct of human subject research projects.
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.
Collaborate with primary investigators, sponsors and research caregivers to plan, conduct and evaluate project protocols, including research subject recruitment.
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.
Maintain study personnel certification records (License, CV, CITI).
Comp
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