Clinical Research Coordinator 244892 - Medix : Job Details

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