Clinical Research Coordinator 244892 Job at Medix™, Merced, CA

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  • Medix™
  • Merced, CA

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)
  • Collaborate with nursing staff for blood draw coordination
  • Maintain direct communication with Principal Investigators and actively manage PI engagement

Qualifications

  • Minimum 2-3 years of clinical research experience
  • Oncology experience is required
  • Bachelor’s degree in a science-related field

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