Clinical Research Coordinator 244892 at Medix™ Merced, CA
Behavioral Health Market Context
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Job Description
nal 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
• 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
Qualifications
- •Minimum 2-3 years of clinical research experience
- •Oncology experience is required
- •Bachelor’s degree in a science-related field
Benefits
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
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