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 while ensuring compliance and data integrity in a remote setting.

Key responsibilities

• Serve as the primary point of contact for investigative sites, providing contextual information on clinical trials and strengthening partnerships
• Conduct site evaluations and training, ensuring adherence to protocols and regulatory standards while promoting effective recruitment and retention strategies
• Monitor study performance and patient safety, proactively identifying risks and implementing corrective action plans as necessary

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, ICH/GCP Guidelines, and therapeutic area indications
• Strong cross-functional collaboration and organizational skills in a dynamic environment
• Ability to leverage technology and resources for customer-centric support at clinical sites