Sandra Dodd is an experienced professional in clinical operations and compliance, currently serving as Associate Director of Clinical Compliance & Records at Amylyx Pharmaceuticals since October 2024. Previously, Sandra held the position of Associate Director, Trial Master File (Lead) at the same company, overseeing TMF Operations. Prior experience includes leadership roles at Xencor and Polaris Pharmaceuticals Inc., focusing on TMF Operations and Clinical Trials Management. Sandra's background also includes significant positions at Eli Lilly and Company, PPD, and Bank of America, demonstrating a diverse skill set across various sectors. Educational credentials feature studies in Clinical Trial & Design Management from UC San Diego Extended Studies, among other institutions.
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