Clinical Research Coordinator II – Translational Trials

Vanderbilt University Medical Center; Nashville (TN); On-site; USD 65,000 - 90,000; Full time

Job summary

Vanderbilt Health in Nashville seeks an experienced research coordinator to oversee regulatory and operational aspects of clinical/translational trials in Allergy, Pulmonary and Critical Care Medicine. You will prepare IRB submissions, amendments and adverse event reports, manage source documents, coordinate site visits, and help ensure compliance with policies and good clinical practice.

This role emphasizes communication with investigators, sponsors, and regulatory authorities, with

Qualifications

• Bachelor’s degree required.
• 1 year of experience in research coordination or similar role.
• Strong understanding of regulatory requirements and Good Clinical Practice.

Responsibilities

• Prepare and process IRB submissions, amendments and adverse event reports.
• Maintain and organize source documentation for audits and sponsor visits.
• Coordinate budget monitoring and invoicing related to studies.
• Serve as liaison between investigators, sponsors and regulatory bodies.

Skills

Communication

Project coordination

Team collaboration

Education

Bachelor’s degree

Job description

Vanderbilt Health in Nashville seeks an experienced research coordinator to oversee regulatory and operational aspects of clinical/translational trials in Allergy, Pulmonary and Critical Care Medicine. You will prepare IRB submissions, amendments and adverse event reports, manage source documents, coordinate site visits, and help ensure compliance with policies and good clinical practice.

This role emphasizes communication with investigators, sponsors, and regulatory authorities, with