Research Coordinator III - RRT/Respiratory
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 III - RRT/Respiratory
Location
Cleveland
Facility
Cleveland Clinic Main Campus
Department
Respiratory Institute Admin-Integrated Hospital Care Institute
Job Code
T99497
Shift
Days
Schedule
8:00am-5:00pm
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 the community. As Research Coordinator III, you are responsible for handling complex trials related to respiratory treatment. Because of these responsibilities, self-drive, organization, time management and a thirst for knowledge are essential. In this position, your team will encourage you and support your growth as you hone your skills in research and management.
A caregiver in this position works days from 8:00AM – 5:00PM.
A caregiver who excels in this role will:
- 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.
Minimum qualifications for the ideal future caregiver include:
- High School Diploma or GED and five years of experience as a Research Coordinator II OR Bachelor’s Degree and three years of experience
- Proficiency with various computer-based skills (word processing, spreadsheets, databases and presentation software)
Preferred qualifications for the ideal future caregiver include:
- Associate’s or Bachelor’s Degree in Healthcare or a science-related field
- Certification as a Registered Respiratory Therapist (RRT)
Our caregivers continue to create the best outcomes for our patients across each of our facilities. Click the link and see how we’re dedicated to providing what matters most to you: https://jobs.clevelandclinic.org/benefits-2/
Personal Protective Equipment:<
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