California Licensed Clinical Research Monitor

Job Summary

A company is looking for a MultiCtr Clin Research Monitor.

Key Responsibilities

• Manage central registration services and ensure compliance with regulatory procedures
• Facilitate external site feasibility review, start-up, and activation for multicenter investigator-initiated trials (IITs)
• Coordinate investigational product shipments and report serious adverse events to regulatory committees

Required Qualifications

• Bachelor's degree in biology, chemistry, biochemistry, physiology, nursing, or related fields
• Two or more years of experience in Clinical Research