Senior Research Coordinator – Eating Disorders Lab

University of Louisville

United States

On-site

USD 48,000 - 72,000

Full time

9 days ago

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Job summary

The University of Louisville's Eating Anxiety and Treatment laboratory in the Department of Psychology seeks a full-time Research Coordinator V to support clinical and observational studies on eating disorders. The role focuses on coordinating protocol activities, maintaining accurate documentation, and ensuring compliance with institutional, federal, and program regulations.

You will work with investigators, staff, and external partners to enhance workflows, monitor quality, and ensure ethical

Qualifications

  • Bachelor's degree in a related field and two years of research experience or equivalent.
  • Experience in regulated research environments (IRB, IACUC, FDA, etc.).
  • Strong communication and documentation skills.

Responsibilities

  • Review proposals and materials for accuracy and compliance.
  • Maintain and update documentation, databases, and records for audits.
  • Coordinate research protocol activities, data collection, and stakeholder communication.
  • Provide guidance on forms, procedures, and regulatory requirements.
  • Assist with assessments, data collection, inspections, and follow-up actions.
  • Collaborate with internal and external stakeholders to support project implementation.
  • Supervise undergraduate and graduate assistants.
  • Perform additional duties as assigned.

Skills

Regulatory compliance
Documentation
Data collection
Communication
Project coordination
Supervision

Education

Bachelor's degree

Tools

SPSS
REDCap
Microsoft Word
Excel
PowerPoint

Job description

The University of Louisville's Eating Anxiety and Treatment laboratory in the Department of Psychology seeks a full-time Research Coordinator V to support clinical and observational studies on eating disorders. The role focuses on coordinating protocol activities, maintaining accurate documentation, and ensuring compliance with institutional, federal, and program regulations.

You will work with investigators, staff, and external partners to enhance workflows, monitor quality, and ensure ethical

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