Over the course of my career, I have cultivated a deep understanding of regulatory standards, compliance requirements, and the intricacies of human subjects research and clinical operations. My specialization lies in optimizing site operations with Sponsor relationships and ensuring efficient bi-directional execution. My aim is to act as a connector between various stakeholders within the clinical research ecosystem, fostering collaborative relationships between Sponsor developmental sciences, translational sciences, clinical science, clinical operations, CROs, Solutions providers, and site leadership. I aspire to be a thought leader in this space, leading discussions and shaping best practices in the management of Sponsor/CRO/Site relationships.