↳PhD in pharmaceutical sciences or related discipline with experience in ADME/DMPK sciences, biopharmaceutics, and modeling and simulation.
↳At least 5+ years in pharmaceutical industry including demonstrated knowledge and experience with PBPK modeling.
↳Hands on experience with PBPK modeling tools such as PK-Sim, Simcyp, or GastroPlus is required.
↳In addition, experience with modeling software such as Monolix, R, Phoenix, or Nonmem is desired.
↳Experience in authoring regulatory documents, knowledge of global regulatory requirements and guidance
↳Broad knowledge of drug discovery and development, e.g., pharmacokinetics, drug delivery, formulation, ADME, DDI, etc.