Experienced Regulatory Affairs professional with over a decade of success leading regulatory compliance and clinical research operations across oncology-focused trials. I specialize in regulatory strategy, study startup, vendor oversight, and cross-functional collaboration to ensure FDA, GCP, and ICH compliance from trial initiation through closeout. With a strong foundation in biotechnology (BS) and regulatory affairs (MS), I bring a scientific and strategic lens to every project. I’ve led initiatives supporting over 40 clinical trials, partnering with top sponsors, CROs, and regulatory bodies to advance innovative therapies with quality and speed. Known for building high-performing teams, streamlining operations, and developing SOPs that elevate compliance standards, I am passionate about bridging science and regulation to drive impactful, patient-centered research. Let’s connect if you’re interested in clinical development, regulatory leadership, or strategic operations in oncology research.