Research Coordinator III

About the role

Join the Cleveland Clinic team, where you will work alongside passionate caregivers and provide patient-first healthcare. Cleveland Clinic is recognized as one of the top hospitals in the nation.

Responsibilities

• Manage complex clinical research activities and oversee key administrative functions related to research trials.
• Track research awards, deadlines, reporting requirements, required documentation, sub-award information, and study-related communications to ensure successful project management and compliance.
• Demonstrate exceptional coordination and compliance with the implementation and conduct of human subject research projects.
• Assist with research study design and protocol development as applicable.
• Independently direct large, complex, multi-center clinical research protocols/programs and coordinate the implementation and conduct of research projects, ensuring adherence to research protocol.
• Report Serious Adverse Events and/or safety as they occur and complete Food and Drug Administration (FDA) and sponsor forms in accordance with GCP guidelines.
• 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.
• Collaborate with primary investigators, sponsors and research caregivers to plan, conduct and evaluate project protocols, including research subject recruitment.
• Maintain study personnel certification records (License, CV, CITI).
• Conduct and document the informed consent process.
• Assist the PI with research study design and development of research protocol.
• Submit the study to appropriate agencies in support of the research programs and assist with annual and other reporting requirements.
• Contribute to or assist with research project budget development.

Requirements

• High School Diploma or GED and five years of experience as a Research Coordinator II or performing the role of a Research Coordinator II
• Or Bachelor’s Degree in a healthcare or science-related field and three years of experience

Qualifications

• Proficient with a variety of computer-based skills (word processing, Outlook, Excel, spreadsheets, databases and presentation software)
• Understanding of the basic concepts of study design

Skills

• Strong self-motivation, organization, time management skills, and a commitment to continuous learning

Benefits

Includes a hybrid work schedule with onsite responsibilities at Main Campus and remote work. A caregiver who excels in this role will:

• Demonstrate exceptional coordination and compliance with the implementation and conduct of human subject research projects.
• Assist with research study design and protocol development as applicable.
• Independently direct large, complex, multi-center clinical research protocols/programs and coordinate the implementation and conduct of research projects, ensuring adherence to research protocol.
• Report Serious Adverse Events and/or safety as they occur and complete Food and Drug Administration (FDA) and sponsor forms in accordance with GCP guidelines.
• 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.
• Collaborate with primary investigators, sponsors and research caregivers to plan, conduct and evaluate project protocols, including research subject recruitment.
• Maintain study personnel certification records (License, CV, CITI).
• Conduct and document the informed consent process.
• Assist the PI with research study design and development of research protocol.
• Submit the study to appropriate agencies in support of the research programs and assist with annual and other reporting requirements.
• Contribute to or assist with research project budget development.

Pay

Minimum Annual Salary: $57,510.00
Maximum Annual Salary: $87,697.50