Research Coordinator III, Cardiovascular Genomics

Cleveland Clinic

Cleveland (OH)

On-site

USD 65,000 - 95,000

Full time

7 days ago
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Job summary

Cleveland Clinic Health System is seeking a Research Coordinator III for the HVTI Center for Cardiovascular Genomics & Data Science at the Cleveland Clinic Main Campus. The role involves overseeing complex cardiovascular research programs, coordinating multi-center protocols and ensuring high-quality data across investigations.

As a key liaison among investigators, sponsors and research administration, you will develop research tools, maintain certifications, and support audits while maintaining

Qualifications

  • 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
  • Proficient with a variety of computer-based skills (word processing, Outlook, Excel, spreadsheets and presentation software)

Responsibilities

  • Demonstrate exceptional coordination and compliance of human subject research projects.
  • Assist with study design and protocol development.
  • Direct large, complex, multi-center clinical research protocols and coordinate implementation and conduct of research projects, ensuring adherence to protocol.
  • Report Serious Adverse Events and/or safety and complete FDA and sponsor forms in accordance with GCP guidelines.
  • Communicate with sponsors, monitors and personnel to ensure study compliance.

Skills

Research coordination
Protocol development
FDA reporting
Regulatory documentation

Education

Bachelor's degree in healthcare or science
High School Diploma or GED

Tools

Excel
Outlook
Databases

Job description

Cleveland Clinic Health System is seeking a Research Coordinator III for the HVTI Center for Cardiovascular Genomics & Data Science at the Cleveland Clinic Main Campus. The role involves overseeing complex cardiovascular research programs, coordinating multi-center protocols and ensuring high-quality data across investigations.

As a key liaison among investigators, sponsors and research administration, you will develop research tools, maintain certifications, and support audits while maintaining

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