Translational Clinical Research Coordinator II

vumc.org; Nashville (TN); On-site; USD 60,000 - 75,000; Full time

Job summary

Vanderbilt Health in Nashville, TN is seeking a Clinical/Translational Research Coordinator II to coordinate approval processes and conduct of clinical/translational research protocols. You will work under guidance to ensure regulatory compliance and data integrity across multiple sites.

The role emphasizes coordinating IRB submissions, maintaining essential documentation, recruiting eligible participants, and supporting trial logistics and invoicing while upholding Good Clinical Practice

Qualifications

• Experience coordinating IRB proposals, amendments, continuing reviews and adverse event reports.
• Maintaining regulatory documents for trials and preparing source documents for audits.
• Screening and recruiting participants and ensuring eligibility criteria are met.

Responsibilities

• Prepare and maintain regulatory documents for trials.
• Identify eligible participants and assist in recruitment.
• Record data on case report forms and ensure accuracy and timeliness.
• Coordinate shipment of specimens per guidelines.
• Support trial invoicing and billing compliance.

Skills

Clinical Research

Study Design

Project Coordination

Communication

Education

Bachelor's degree

Job description

Vanderbilt Health in Nashville, TN is seeking a Clinical/Translational Research Coordinator II to coordinate approval processes and conduct of clinical/translational research protocols. You will work under guidance to ensure regulatory compliance and data integrity across multiple sites.

The role emphasizes coordinating IRB submissions, maintaining essential documentation, recruiting eligible participants, and supporting trial logistics and invoicing while upholding Good Clinical Practice