Step into a key role as an Oncology Clinical Research Associate, managing trial sites and ensuring compliance with study protocols. Focus on patient safety and quality execution.

In this position, you will be responsible for overseeing all aspects of clinical trial management, including monitoring investigator sites’ compliance with Good Clinical Practices (GCP). You'll work closely with Site Care Partners and study teams to resolve issues and support site personnel training. Your background in clinical research will be fundamental in ensuring smooth operations and the timely execution of trial objectives.

Key Responsibilities:
• Manage clinical trial activities at investigator sites effectively
• Ensure thorough adherence to applicable regulations and best practices
• Serve as a communication hub for investigator sites and study teams
• Monitor adverse events and collaborate with safety units
• Support site staff in understanding...