A caregiver who excels in this role will:

• 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.

Minimum qualifications for the ideal future caregiver include:

• High school diploma or GED.

• Two years of experience as a Research Coordinator or healthcare experience.

• OR Bachelor’s/Associates degree may substitute for two years of the experience requirement.

• Show proficiency with various computer-based skills (word processing, spreadsheets, databases and presentation software).

Preferred qualifications for the ideal future caregiver include:

• Bachelor’s degree in healthcare or a science-related field.

Our caregivers continue to create the best outcomes for our patients across each of our facilities. Click the link and see how we’re dedicated to providing what matters most to you: https://jobs.clevelandclinic.org/benefits-2/

Physical Requirements: