Rheumatology Research Coordinator II | Hybrid Trials

Cleveland Clinic; Cleveland (OH); Presencial; USD 65.000 - 90.000; Jornada completa

Descripción de la vacante

Cleveland Clinic Main Campus is seeking a Research Coordinator II for Rheumatology to enroll patients in clinical trials, conduct study visits and collect questionnaires. You will independently manage 10–15 prospective studies, including drug and device trials, across the study lifecycle with support from a collaborative team.

The role requires coordinating regulatory documents, data capture and safety reporting, with potential transition to hybrid work based on performance.

Formación

• Requires high school diploma or GED with 3 years as Research Coordinator I or equivalent.
• OR an Associate/Bachelor's in health care or science with 1 year as Research Coordinator I or equivalent.
• Proficient with word processing, spreadsheets, database and presentation software.

Responsabilidades

• Coordinate 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 log serious adverse events and/or safety issues.
• Communicate with sponsors, monitors and research personnel to ensure study compliance.
• Serve as liaison between investigators, study personnel and central research offices for protocol interpretation and enrollment.
• Schedule site visits, initiations, webinars, monitoring and close-out visits.
• Support planning, conduct and evaluation of project protocols and recruitment.

Conocimientos

Study coordination

Regulatory submissions

Data management

Communication

Educación

High School Diploma or GED

Associate/Bachelor's in health care or science

Herramientas

Word processing

Spreadsheets

Database software

Presentation software

Descripción del empleo

Cleveland Clinic Main Campus is seeking a Research Coordinator II for Rheumatology to enroll patients in clinical trials, conduct study visits and collect questionnaires. You will independently manage 10–15 prospective studies, including drug and device trials, across the study lifecycle with support from a collaborative team.

The role requires coordinating regulatory documents, data capture and safety reporting, with potential transition to hybrid work based on performance.