Clinical Research Coordinator II: Translational Trials

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

Job summary

Vanderbilt Health’s GI Medicine Clinical Trials program is seeking a Clinical Translational Research Coordinator II to oversee regulatory activities and the coordination of multiple clinical studies. You will manage IRB submissions, maintain essential study documentation, and support audits and inspections.

The role involves screening and enrolling participants, coordinating study logistics, and ensuring data integrity across CRFs while upholding Good Clinical Practice and human subjects

Qualifications

• Prepare, submit, and manage regulatory documents including IRB adverse event reports.
• Maintain essential regulatory, sponsor, and study documentation for audit readiness.
• Coordinate study operations across multiple trials; procure equipment and resources.
• Screen, recruit, consent, and enroll participants per protocol.
• Ensure data quality and regulatory compliance in case report forms.

Responsibilities

• Regulatory management and IRB submissions for multiple studies.
• Site start-up, sponsor communications, and regulatory inspections support.
• Participant recruitment, consent, and retention across trials.
• Data entry, query resolution, and regulatory documentation maintenance.

Skills

Regulatory affairs

IRB submissions

GCP adherence

Data management

Study coordination

Participant recruitment

Education

Bachelor's degree in a related field

Job description

Vanderbilt Health’s GI Medicine Clinical Trials program is seeking a Clinical Translational Research Coordinator II to oversee regulatory activities and the coordination of multiple clinical studies. You will manage IRB submissions, maintain essential study documentation, and support audits and inspections.

The role involves screening and enrolling participants, coordinating study logistics, and ensuring data integrity across CRFs while upholding Good Clinical Practice and human subjects