Clinical Research Associate II

Job Summary

To advance clinical research excellence, the full-time Clinical Research Associate II will manage site evaluations, training, and monitoring activities remotely, ensuring compliance and data integrity in neuro and immunology trials.

Key responsibilities

• Serve as the primary contact for investigative sites, providing contextual information and strengthening partnerships
• Conduct site evaluations, training, and monitoring to ensure adherence to protocols and regulatory standards
• Develop site engagement strategies and assess recruitment techniques to enhance study performance and patient safety

Required qualifications

• 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 cross-functional collaboration and organizational skills
• Ability to leverage technology and tools for effective site engagement and support