Under the guidance of the Regulatory Manager and Regulatory Coordinator, the Regulatory Assistant supports the development, implementation and regulatory compliance maintenance of clinical research trials for multiple sites and studies of different therapeutic areas and phases in accordance with appropriate regulations, Standard Operating Procedures (SOP'S), and study specific protocols/plans and processes. The Regulatory Coordinator will be required to complete Good Clinical Practices (GCP) training, and additional specialized regulatory training, sponsor training on protocol requirements, etc.