Join Cleveland Clinic’s Heart, Vascular and Thoracic Institute to become a part of one of the most respected healthcare organizations in the world. This center cares for patients with a variety of heart, vascular and thoracic diseases, providing the most advanced treatments in a welcoming environment. Here, you can build a rewarding career, enhance your skills and develop life-long relationships with fellow caregivers.
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. As Research Coordinator III in the Heart, Vascular and Thoracic Institute, you will be responsible for supporting our Electrophysiology (EP) Research Section through implementing and conducting high complexity human subject research projects. Because of these responsibilities, self-drive, organization, time management and a thirst for knowledge are essential. Come be a part of an environment of belonging—where everyone is valued and respected—dedicated to collaboration, mentorship, diversity and inclusion.
A caregiver in this position works days from 8:00AM – 5:00PM.

A caregiver who excels in this role will:

• Independently direct large, complex, multi-center clinical research protocols and programs.
• Coordinate the implementation and conduction of human subject research projects, ensuring adherence to research protocol requirements.
• Maintain regulatory documents and binders, conduct data management, complete IRB submissions, communicate with the research team and develop data capture and monitoring plans.
• 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
• Five years of experience as a Research Coordinator II
• 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. A Bachelor’s Degree may substitute for two years of the experience requirement

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/

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

• Independently direct large, complex, multi-center clinical research protocols and programs.
• Coordinate the implementation and conduction of human subject research projects, ensuring adherence to research protocol requirements.
• Maintain regulatory documents and binders, conduct data management, complete IRB submissions, communicate with the research team and develop data capture and monitoring plans.
• 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