Clinical Research Coordinator 243335 Job at Medix™, Sarasota, FL

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  • Medix™
  • Sarasota, FL

Job Description

Key Responsibilities:

  • Manage regulatory submissions, including IRB documentation
  • Serve as the primary point of contact for sponsors (excluding budget and contracting)
  • Conduct informed consent discussions with patients
  • Coordinate scheduling for standard-of-care procedures
  • Ensure accountability and compliance for Investigational Products (IP)
  • Maintain direct communication with Principal Investigators and actively manage PI engagement

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