Clinical Research Associate II

Job Summary

To advance clinical research in oncology, the full-time Clinical Research Associate II will manage site evaluations, training, and monitoring activities remotely, ensuring compliance with protocols and enhancing study performance.

Key responsibilities

• Serve as the primary contact for investigative sites, providing guidance on clinical trials and strengthening partnerships
• Conduct site evaluations, training, and monitoring to ensure adherence to protocols and regulatory standards
• Implement customized site engagement strategies to improve recruitment, retention, and overall study compliance

Required qualifications

• Appropriate tertiary qualification in health-related disciplines (Medical, Scientific, Nursing) preferred
• Minimum of 1 year of clinically related experience, including 6 months in clinical research monitoring
• Advanced knowledge of regulatory requirements and ICH/GCP Guidelines
• Strong planning and organizational skills to manage competing projects effectively
• Ability to leverage technology and tools for customer-centric support in clinical settings