Anne-Marie Manasier is a clinical research and business development leader with more than 22 years of experience across the CRO and clinical research site environments. Her background includes clinical operations, site identification and selection, feasibility, protocol execution, investigator due diligence, and building strong relationships among sponsors, CROs, and research sites.
While currently the Director of Business Development at hyperCORE International, Anne-Marie’s vast experience in clinical oversight brings a practical, operations-focused perspective to clinical research and regulatory readiness. Her experience includes evaluating site capabilities, processes, documentation, and operational practices that contribute to successful trial execution and inspection preparedness. She is passionate about helping research sites strengthen their operational foundations, proactively identify risks, and maintain a state of readiness for FDA inspections.
She is thrilled to be facilitating this year’s “Regulatory Readiness: FDA Inspections” presentation at SCRS.