Research Coordinator II
| Company | Cleveland Clinic |
|---|---|
| Location | Weston, FL, USA |
| Salary | $Not Provided – $Not Provided |
| Type | Full-Time |
| Degrees | Bachelor’s, Associate’s |
| Experience Level | Mid Level |
Requirements
- High School Diploma/GED and three years of experience as a Research Coordinator I or performing the role of a Research Coordinator I OR Associate’s or Bachelor’s Degree in Healthcare or a science-related field and one year of experience
- Demonstrated proficiency with a variety of computer-based skills, especially in the use of word processing, spreadsheets, database and presentation software
Responsibilities
- Coordinate the implementation and conduct of research projects, ensuring adherence to research protocol requirements (e.g., timely completion and communication of regulatory documents, the development of data capture and monitoring plans, reporting of Serious Adverse Events, completion of Food and Drug Administration (FDA) and sponsor forms, etc.)
- 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
- 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
- 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
- Assist with the development of training and educational material for assigned research protocols
- Provide and document education as needed
- Conduct and document the informed consent process
- Assist with research project budget development as needed
Preferred Qualifications
- Associate’s or Bachelor’s Degree in Healthcare or a science-related field