Research Coordinator I - Pediatric Cardiology

Cleveland Clinic•Cleveland, OH

1d•Onsite

About The Position

Join Cleveland Clinic’s Main Campus where research and surgery are advanced, technology is leading-edge, patient care is world class and caregivers are family. Here, you will work alongside a passionate and dedicated team, receive endless support and appreciation, and build a rewarding career with one of the most respected healthcare organizations in the world. As Research Coordinator I, your role is crucial in enrolling patients in clinical trials, conducting study visits, and collecting questionnaires with important study-related information. In this role, you will work with investigators across the Cardiology Department on a variety of research, including registries, sponsored studies, and drug and device trials. You will enroll patients ranging from newborns to adults, complete study paperwork and consent documentation, and receive 12–16 weeks of training alongside an experienced team member to support your transition into the role. While numerous responsibilities can be difficult to juggle at times, your team will encourage you to enhance your skills and improve your ability to identify new avenues of treatment. Come join a culture devoted to pushing the needle forward in healthcare. A caregiver in this position works Monday through Friday from 8:00 a.m. – 5:00 p.m.

Requirements

High School Diploma or GED and two years of clinical research or healthcare experience OR Associate’s or Bachelor’s Degree in a healthcare or a science-related field
Demonstrated proficiency with various computer-based skills (word processing, spreadsheets, databases, presentation software, data entry, and EPIC)
Understanding of the basic concepts of study design
Within 90 days of hire, must successfully complete certification in Human Subjects Research as required by the Responsible Conduct of Research guidelines adopted by Cleveland Clinic
Strong organizational, communication and interpersonal skills

Nice To Haves

Associate’s or Bachelor’s Degree in a healthcare or a science-related field

Responsibilities

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.
Complete certification in Human Subjects Research as required by the Responsible Conduct of Research guidelines adopted by Cleveland Clinic.