California Licensed Clinical Research Associate

Job Summary

A company is looking for a Clinical Research Associate (CRA) II.

Key Responsibilities

• Conduct Phase I-IV clinical studies in compliance with Federal Regulations and ICH guidelines
• Assist in planning study conduct, including CRF design and CRO management
• Monitor investigational sites to ensure protocol adherence and timely patient enrollment

Required Qualifications

• Experience in clinical research, specifically in Phase I-IV studies
• Knowledge of Federal Regulations and ICH guidelines
• Ability to manage and train investigator sites
• Experience in data management and CRF processing
• Contract employment availability