III - Oncology

Cleveland Clinic

1d•Hybrid

About The Position

Join the Cleveland Clinic Taussig Cancer Institute where more than 250 highly skilled healthcare professionals provide advanced cancer care to thousands of patients each year. This team focuses on a wide variety of services and innovations, including clinical trials and internationally-recognized research efforts. Here, you will work with the latest technologies, gain hands-on experience, receive endless support and build a rewarding career with one of the most respected healthcare organizations in the world. As a Clinical Research Coordinator for the Head and Neck program group, you will play a vital role in advancing oncology research and improving treatment options for cancer patients. In this role, you will enroll patients in clinical trials, schedule and conduct study visits, and collect important study-related information, including vital signs and quality-of-life questionnaires. You will also assist patients throughout their treatment journey by processing reimbursements, supporting group visits, and performing Clinical Research Coordinator I responsibilities to ensure seamless study operations. Through your work, you will help advance oncology research and provide patients with access to new and potentially life-changing therapies when other treatment options may be limited.

Requirements

High School Diploma or GED and three years of experience as a Research Coordinator I OR Associate’s or Bachelor’s Degree in a healthcare or a science-related field and one year of experience
Demonstrated proficiency with a variety of computer-based skills (word processing, spreadsheets, databases and presentation software)
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

Nice To Haves

Associate’s or Bachelor’s Degree in Healthcare or a science-related field
Clinical background

Responsibilities

Coordinate 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.
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.