Research Coordinator I NE

Cleveland Clinic

5d•Onsite

About The Position

Join the Cleveland Clinic Florida team at the Krupa Center in Weston, where you will work alongside highly skilled and compassionate caregivers and board-certified family practice physicians to provide patient-first healthcare. Cleveland Clinic is consistently recognized as one of the top hospitals in the nation, offering quality preventive care, management of chronic conditions and comprehensive services for the entire family. At Cleveland Clinic, you will receive strong support and recognition, collaborate with dedicated professionals and build a rewarding career with one of the world’s most respected healthcare organizations. As Research Coordinator II, you will help manage the DDSI clinical research department and its activities while coordinating the compliant implementation and conduct of human subject research projects, typically involving a low workload and low complexity. While the numerous responsibilities can be difficult to juggle at times, your team will encourage you to enhance your skills and strengthen your ability to identify new avenues of treatment to support research and education within DDSI. A caregiver in this position works days from 7:30 a.m. -- 4:30 p.m.

Requirements

High school diploma or GED
Two years of clinical research or healthcare experience
Proficiency with various computer-based skills (word processing, spreadsheets, databases and presentation software)

Nice To Haves

Bachelor’s degree in healthcare or a science-related field. This may substitute for two years of the experience requirement

Responsibilities

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.
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.