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May 11
Own and support GxP applications for R&D and regulated functions, leading system configuration, validation, releases, compliance documentation, and cross-functional improvements with business, Quality, and vendor partners.
Own and support GxP applications for R&D and regulated functions, leading system configuration, validation, releases, compliance documentation, and cross-functional improvements with business, Quality, and vendor partners.
Leads toxicology, safety pharmacology, and translational science across programs, shaping nonclinical strategies and studies, supporting regulatory submissions, and advancing assets from discovery through early clinical development.
Leads early-development clinical strategy and study execution, shaping plans and designs, authoring key clinical documents, interpreting data, and guiding cross-functional teams to deliver scientifically rigorous trials.
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