Ketaki Pendse

Background

About Ketaki Pendse

A seasoned Clinical Research Professional with over 15 years of expertise in clinical trial management, centralized monitoring, and risk-based monitoring across Oncology, Infectious Disease, Nephrology, and CNS. Proficient in RBM, RBM+, and Non-RBM projects, with a strong focus on clinical trial operations, investigator payments, vendor management, and risk analysis. As a Centralized Monitoring Lead at IQVIA, I oversee e-TMF management, data interpretation, forecasting team hours, and ensuring regulatory compliance while driving efficiency in clinical research processes. My leadership approach emphasizes mentorship, problem-solving, and adaptability to fast-paced changes in the evolving clinical landscape. Passionate about streamlining operations and enhancing data-driven decision-making, I excel in collaborating with cross-functional teams to deliver high-quality clinical trials. Always open to networking, industry discussions, and thought leadership, I aim to contribute to the continuous evolution of clinical research and patient-centric solutions. Let’s connect and collaborate!