Clin/Trans Research Coordinator 3
On-site · Nashville, Tennessee, United States
Job Summary
Coordinate the approval processes and conduct of clinical/translational research protocols to maintain integrity and quality, prepare and maintain regulatory documents, recruit and screen participants, schedule and organize study visits and assessments, manage data collection and source documentation, handle study specimens, support budgeting and invoicing, ensure compliance with regulations and good clinical practice, and communicate with investigators, sponsors, and study personnel to drive successful trial operations.
Required Qualifications
- Bachelor's degree
- 3 years relevant work experience in clinical/translational research
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