Clinical Research Site Liaison II

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