Medix
Job Location : Merced,CA, USA
Posted on : 2025-09-01T09:14:50Z
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