Cleveland Clinic - Cleveland, OH

posted 2 months ago

Full-time - Entry Level
Remote - Cleveland, OH
Ambulatory Health Care Services

About the position

Join Cleveland Clinic's Lerner Research Institute as a Research Coordinator II in the Clinical Research Unit, where you will be part of a highly respected healthcare organization known for its commitment to research, innovation, and education. The Lerner Research Institute is dedicated to conducting leading-edge research that enhances patient care both now and in the future. The M51 Clinical Research Unit fosters a unique culture that prioritizes the well-being of its caregivers, both professionally and personally, while continuously striving for better healthcare outcomes. This position offers numerous opportunities for professional development and career advancement, as you will be involved in various clinical trials and collaborate with multiple institutes across Cleveland Clinic, providing extensive networking and growth opportunities. As a Research Coordinator II, you will work from 8:00 AM to 4:30 PM, with the flexibility to work from home two days a week. Your primary responsibilities will include coordinating the compliant implementation and conduct of human subject research projects, which typically involve medium workload and complexity. You will maintain regulatory documents and binders, manage data, complete Institutional Review Board (IRB) submissions, and communicate effectively with the research team. Additionally, you will report and complete serious adverse events and safety logs, ensuring compliance with all study aspects by liaising with sponsors, monitors, and research personnel. Your role will also involve scheduling pre-site selection visits, site initiation visits, webinars, monitoring, and close-out visits. You will plan, conduct, and evaluate project protocols and research subject recruitment, monitor project status, and report research data. Completing regulatory documents, data capture, monitoring plans, and protocol-related activities will be essential, as will assisting with audits and maintaining research tools.

Responsibilities

  • Coordinate the compliant implementation and conduct of human subject research projects, typically of medium workload and medium complexity.
  • Maintain regulatory documents and binders, conduct data management, complete IRB submissions and communicate with the research team.
  • Report and complete serious adverse events and/or safety logs.
  • 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.
  • Schedule pre-site selection visits, site initiation visits, webinars, monitoring 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 preparing and responding to audits and maintaining research tools.

Requirements

  • High school diploma or GED.
  • Three years of experience as a Research Coordinator I.
  • Demonstrated proficiency with a variety of computer-based skills (word processing, spreadsheets, databases and presentation software).

Nice-to-haves

  • Associate's or bachelor's degree in healthcare or a science-related field. This may substitute for two years of the experience requirement.

Benefits

  • Healthcare insurance
  • Dental insurance
  • Vision insurance
  • Retirement plan
  • Professional development opportunities
  • Flexible work schedule (work from home two days a week)
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service