Travel-Ready Clinical Research Regulatory Coordinator

Us Uro; Tennessee; Hybrid; USD 65,000 - 85,000; Full time

Benefits offered by this job

Medical benefits

HSA/FSA

401(k) matching

Employee assistance program

Job summary

Central Ohio Urology Group seeks a Clinical Research Regulatory Coordinator to maintain regulatory documents and ensure ICH-GCP adherence across sites. You will support staff documentation, certifications, and site readiness for inspections, while coordinating IRB submissions and continuing reviews.

The role requires 2–5 years of clinical research experience, strong communication, superb organizational skills, and willingness to travel to multiple sites.

Qualifications

• 2-5 years of clinical research experience is desirable.
• Bachelor's degree in a related field is required.
• Proficiency in Microsoft Office (Word, Excel) is expected.
• Willing and able to travel to other sites to ensure regulatory compliance.

Responsibilities

• Organize and maintain study documents.
• Oversee staff and site related documentation and certifications.
• Ensure regulatory compliance by all sites to ICH-GCP guidelines and site operating procedures.
• Prepare site for regulatory inspections.
• Submit continuing review reports and new study IRB submissions.
• Travel to U.S. Urology sites to review regulatory documentation.

Skills

Clinical research

Regulatory knowledge

Documentation management

Communication

Travel readiness

Education

Bachelor's degree in related field

Tools

Microsoft Office

Job description

Central Ohio Urology Group seeks a Clinical Research Regulatory Coordinator to maintain regulatory documents and ensure ICH-GCP adherence across sites. You will support staff documentation, certifications, and site readiness for inspections, while coordinating IRB submissions and continuing reviews.

The role requires 2–5 years of clinical research experience, strong communication, superb organizational skills, and willingness to travel to multiple sites.