Cancer Research Coordinator II — Hybrid Eligible

Cleveland Clinic; West Lindsey; On-site; GBP 48,000 - 67,000; Full time

Job summary

Cleveland Clinic Health System is seeking a Research Coordinator II at Weston Family Health Center to support the Cancer Research Group. The role involves coordinating compliant clinical trial activities, start-up tasks, patient visits, and regulatory document handling in a medium workload environment.

Responsibilities include liaising with investigators, sponsors and central offices, developing monitoring plans, and ensuring timely regulatory submissions.

Qualifications

• Three years of clinical research experience
• Bachelor’s degree in healthcare or science field and one year of clinical research experience
• Demonstrated basic computer proficiency
• Strong organizational, communication and interpersonal skills
• Within 90 days of hire, must complete Human Subjects Research certification

Responsibilities

• Coordinate implementation and conduct of research projects ensuring adherence to protocol
• Serve as liaison between investigators, study staff and central research offices
• Collaborate with investigators, sponsors and staff on study planning and execution
• Monitor and report project status
• Assist with regulatory documents and audits
• Develop training material for research protocols
• Conduct informed consent process
• May assist with budget development
• Other duties as assigned

Skills

Clinical research

Regulatory knowledge

Data capture

Communication

Education

Bachelor’s degree in healthcare or science

3 years clinical research experience

Tools

Microsoft Office

Job description

Cleveland Clinic Health System is seeking a Research Coordinator II at Weston Family Health Center to support the Cancer Research Group. The role involves coordinating compliant clinical trial activities, start-up tasks, patient visits, and regulatory document handling in a medium workload environment.

Responsibilities include liaising with investigators, sponsors and central offices, developing monitoring plans, and ensuring timely regulatory submissions.