Clinical Research Coordinator: Regulatory & Study Ops

Mercy Health; Toledo (OH); On-site; USD 55,000 - 80,000; Full time

Benefits offered by this job

Competitive pay

Benefits package

Paid time off

Tuition assistance

Job summary

Mercy Health in Toledo, OH is seeking a Research Coordinator to support projects across Mercy Health System. You will recruit and monitor participants, coordinate regulatory documents, and assist investigators in developing research studies, ensuring adherence to federal regulations and ICH/GCP guidelines.

The role involves data management, budgeting assistance, collaboration with departments, and presenting findings.

Qualifications

• Prior clinical research experience and understanding of the scientific process preferred.
• Ability to write, follow and monitor study protocols and informed consent documents.
• Excellent written and oral communication and data handling skills.

Responsibilities

• Coordinate regulatory documents and ensure protocol compliance with FDA/ICH/GCP.
• Assist with IRB submissions, amendments and annual reports.
• Assist with grant and study budget applications.
• Recruit and screen subjects and inform care teams of study status.
• Maintain research files, collect observational data, and manage data entry.

Skills

Clinical research

Regulatory knowledge

Data management

Documentation skills

Team collaboration

Education

2 Year/Associates Degree

4 Year/Bachelors Degree

Job description

Mercy Health in Toledo, OH is seeking a Research Coordinator to support projects across Mercy Health System. You will recruit and monitor participants, coordinate regulatory documents, and assist investigators in developing research studies, ensuring adherence to federal regulations and ICH/GCP guidelines.

The role involves data management, budgeting assistance, collaboration with departments, and presenting findings.