Clinical Research Coordinator III
Job Summary
The We Grow Healthy Center at Monroe Carrel Jr. Children’s Hospital at Vanderbilt is recruiting an experienced, highly motivated research coordinator to take a leading role in a multi-site clinical trial (DOSE Trial; NCT06654323) focused on improving child and family health. This role will support a program of research focused on developing, implementing, and evaluating practical, evidence-based interventions that promote healthy behaviors and prevent chronic disease.
What Makes This Role Different
Leadership: Serve as the operational lead for a multi-site clinical trial
Autonomy with support: High independence alongside close collaboration with faculty and senior staff
Impact: Work directly connected to improving child and family health in real-world settings
Growth: Opportunities to contribute to manuscripts, grants, and cross-project collaborations
Key Responsibilities
Lead daily study operations; coordinate activities across multiple clinical sites
Serve as the central communication point between investigators, site teams, and collaborators
Facilitate steering committee and investigator meetings
Troubleshoot site challenges and ensure milestone completion
Prepare and oversee IRB submissions, amendments, continuing reviews, and adverse event reporting
Maintain protocol adherence across all sites
Update manuals of operations and ensure compliance with institutional and federal regulations
Oversee REDCap database development and maintenance
Train staff in data entry procedures
Conduct routine data quality checks
Coordinate with biostatistics teams
Supervise research assistants, coordinators, and interns
Conduct onboarding, training, and performance feedback
Foster a collaborative team culture
Oversee recruitment and consent workflows
Build relationships with participating families and community partners
Support culturally responsive communication (Spanish language skills preferred)
Aid with progress reports, manuscripts, abstracts, and grant-related materials
Contribute to cross-project collaborations within the research group
Required Qualifications
Bachelor’s degree (or equivalent experience)
At least 3 years of research experience (5+ years preferred)
Experience working with IRBs and regulatory processes
Experience working with pediatric populations
Strong organizational, communication, and problem-solving skills