III - Cancer Center

Cleveland Clinic•Independence, MO

2d•Hybrid

About The Position

The Research Coordinator works with Cleveland Clinic’s Taussig Cancer Institute, supporting clinical trials and cancer research. The role coordinates the compliant implementation and conduct of human-subject research, including patient enrollment, study visits, questionnaire collection, regulatory documentation, data management, and communication with research teams and external study personnel. The position is described as Research Coordinator II in the role details, although the listed job title includes levels I, II, and III. The position follows a hybrid schedule, with the option to work onsite two days per week and remotely three days per week. The stated schedule is 8:00 a.m. to 4:30 p.m. The role may require irregular hours.

Requirements

High school diploma or GED and three years of experience as a Research Coordinator I or performing the role of a Research Coordinator I; alternatively, an associate or bachelor's degree in a healthcare- or science-related field and one year of experience as a Research Coordinator I or performing that role.
Proficiency with computer-based skills, including word processing, spreadsheets, database, and presentation software.
Understanding of basic study-design concepts.

Nice To Haves

Associate or bachelor's degree in a healthcare- or science-related field.
Research experience.

Responsibilities

Coordinate compliant implementation and conduct of human-subject research projects.
Maintain regulatory documents and binders, manage data, complete IRB submissions, and communicate with the research team.
Report and complete serious adverse events and safety logs.
Communicate with sponsors, monitors, and research personnel to ensure study compliance.
Serve as a liaison among investigators, research personnel, outside study personnel, and central research administration offices on protocol interpretation, enrollment, and safety questions.
Schedule pre-site selection visits, site initiation visits, webinars, monitoring visits, 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 audit preparation and responses, and maintain research tools.
Enroll patients in clinical trials, conduct study visits, and collect study-related questionnaires and information.