Clinical Research Site Liaison II

Job Summary

Managing day-to-day activities for external sites participating in early phase oncology clinical research trials, the full-time Clinical Research Site Liaison II will ensure compliance with federal regulations and Moffitt's standards while overseeing trial execution, enrollment, and data collection in a remote environment.

Key responsibilities

• Oversee the life cycle of clinical research projects, ensuring compliance with regulatory standards and internal processes
• Monitor site performance during trials, including enrollment, safety event reporting, and data collection
• Identify and address trends in trial execution to enhance site performance and compliance

Required qualifications

• Associates Degree with 5 years of clinical trials experience, or a Bachelor's Degree with 3 years of experience, or a Master's Degree with 1 year of multi-site clinical trials experience, preferably in oncology
• Experience in patient-facing coordination, data management, or regulatory activities
• Knowledge of clinical research regulations and processes
• Experience working in multi-site clinical trial environments