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Clinical Research Coordinator in Tampa, FL at TeamHealth

Date Posted: 7/23/2018

Job Snapshot

Job Description

The Clinical Research Coordinator is responsible for grant acquisition, protocol writing / editing, IRB submission, data collection/ statistical analysis, paper writing/editing, presentations and publication processes for multiple studies.

Under the direction and supervision of the Director of Research, the Clinical Research Coordinator assumes responsibility for the following:

  • Undergraduate, graduate, and medical student vetting, recruitment, credentialing, and training.
  • Patient interaction:  subject recruitment, retention, and the informed consent process.



Job Requirements


  • Bachelors of Science or equivalent degree
  • 1 – 2  years of productive academic or clinical research
  • Comprehensive understanding of IRB study requirements, the submission process to, and FDA requirements for Phase I – III drug testing and proving Substantial Equivalence for medical devices.  

Strongly Preferred:

  • HIPPA certified
  • IATA certified for the shipping of dry ice and hazardous biological reagents
  • CITI certified for:
    • IRB
    • research ethics
    • clinical research
    • record review
    • general lab safety
    • biological reagents