Research Coordinator III - Respiratory

Cleveland Clinic

23h•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. 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. Innovative research and groundbreaking discoveries happen every day at Cleveland Clinic. We are creating an environment of belonging—where everyone is valued and respected—dedicated to collaboration, mentorship, diversity and inclusion. As a Research Coordinator III, you will join a multi-disciplinary, talented team to coordinate the compliant implementation and conduct of human subject research projects, typically of high workload and high complexity. A caregiver in this position works from 8:00AM - 4:30PM

Requirements

High School Diploma or GED
Five years experience as a Research Coordinator II or performing the role of a Research Coordinator II.
Bachelor's degree in health care or science related field may offset two years of experience requirement.
Demonstrated proficiency with a variety of computer-based skills (word processing, spreadsheets, databases and presentation software)

Nice To Haves

Associate’s or bachelor’s degree in healthcare or a science-related field

Responsibilities

Coordinate the implementation and conduct of research projects ensuring adherence to research protocol requirements which may include maintenance of regulatory documents and binders, data management, IRB submissions and communication of such to the research team.
Communicate with sponsors, monitors, research personnel to ensure all aspects of study compliance.
Collaborate with study team to schedule pre-site selection visits, site initiation visits, webinars, monitoring, and close-out visits.
Collaborate with primary investigator, sponsor, and research staff to plan, conduct, and evaluate project protocols, including research subject recruitment.
Monitor and report project status.
Complete regulatory documents, data capture and monitoring plans.
Complete protocol related activities.
Monitors research data to maintain quality.
Develop and maintain knowledge of research protocols to coordinate the comprehensive and compliant execution of assigned protocols.
Assist with preparation for audits and response to audits.
Assis in the development and maintenance of research tools, such as spreadsheets, questionnaires, and/or brochures.
Maintain personnel certification records (License, CV, CITI).
Maintain professional relationships, including frequent and open effective communication with internal and external customers.
Document the education and training of research personnel as needed.