Clinical Research Coordinator 244892 at Medix™ Merced, CA

Job Description

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