Senior Clinical Research Associate

Job Summary

Senior Clinical Research Associate, a full-time salaried position requiring 3 years of experience, responsible for site management, data quality assurance, and compliance with clinical trial protocols.

Key Responsibilities

• Provide site management and support to trial staff from initiation to closeout
• Ensure high-quality data collection and compliance with regulatory standards
• Train external trial staff on various reporting and monitoring processes

Required Qualifications

• BA/BS or higher educational requirement
• Minimum of 3 years of CRA monitoring experience from sponsor or CRO
• Ideally 4+ years of field CRA monitoring experience for drug trials
• 6+ years of industry experience in clinical research
• Remote monitoring experience and risk-based monitoring experience preferred