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Responsible for leading non‑clinical and early clinical pharmacology strategy across drug development programs. Provides expertise in PK/PD, modeling & simulation, and Model‑Informed Drug Development (MIDD) to support dose selection, study design, and
The successful candidate will serve as Lumis' medical device regulatory subject matter expert, leading project delivery, supporting business growth, enhancing industry visibility, and further developing the Lumis brand as a recognized provider of medical
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