A seasoned clinical trial professional and healthcare executive with a robust twenty-five-year track record, specializing in compliance, protocol development, bioethics, quality principles, operations, and the implementation of pragmatic solutions for intricate systemic challenges. Demonstrates expertise in designing clinical research governance platforms, acknowledging the integral connection between trials and the clinical care ecosystem. Recognizes the nuanced bidirectional dependencies of data and regulations at the local, state, and federal levels. Possesses a comprehensive background encompassing clinical care, grant administration, leadership, compliance, fiscal management, Institutional Review Board (IRB) oversight, and operations in diverse settings, including private institutions, academia, federal agencies, state organizations, and startup environments. Proven ability to optimize throughput and efficiency across various facets of clinical trial management.

Session:

• When Corrective and Preventive Action Plans Fail: Fixing Repeat Findings