California Licensed Principal Clinical Research Coordinator

Job Summary

A company is looking for a Principal Clinical Research Coordinator.

Key Responsibilities

• Serve as the primary contact between study sponsors, investigators, and research teams, managing inquiries and trial coordination
• Oversee operational execution of studies, including patient registration, randomization, and study close-out activities
• Ensure regulatory compliance and accurate documentation across various systems, and manage safety and sponsor reporting requirements

Required Qualifications

• Bachelor's degree in science, health, or a related field from an accredited university
• 5-7 years of research or relevant experience
• Experience with CTMS, EMR, and eRegulatory Systems
• Working knowledge of clinical trials and relevant regulations
• Certification in Good Clinical Practice (GCP) and Human Subjects Protection (HSP) within the first month of employment; SOCRA or ACRP Certification within two years