Senior Scientist Translational Adme

Johnson & Johnson Johnson & Johnson · Pharma · Beerse, Antwerp, Belgium

Senior Scientist Translational ADME role at Johnson & Johnson focused on advancing clearance predictions using novel in vitro–in vivo extrapolation (IVIVE) and mechanistic modeling approaches for small molecules and other emerging modalities. Requires hands-on lab work with ex vivo and in vitro liver models, bioanalytical assay development, and quantitative mechanistic modeling. The role involves scientific leadership, authoring reports, and presenting data internally and externally.

What you'd actually do

  1. Employing sophisticated ex vivo techniques and complex in vitro models (CIVM), developing innovative in vitro methods and mechanistic modelling approaches to enhance our understanding of transporter and enzyme interplay and their contribution to hepatic clearance and DDI.
  2. Strengthening translational ADME capabilities, specifically advancing clearance predictions through novel in vitro–in vivo extrapolation (IVIVE)approaches for small molecules and other emerging modalities such as degraders, RipTacs, and peptides.
  3. Authoring reports and scientific publications and present data to the scientific community both internally and externally.
  4. Providing project teams with mechanistic understanding and integrated interpretation of in vitro and in vivo ADME properties, drug-drug interaction (DDI) liabilities (enzymes and transporters), and the relationship between PK/toxicokinetics and PD response to support key decisions for discovery and development projects.

Skills

Required

  • PhD in Pharmaceutical Sciences, Biology, Pharmacology, Biomedical Sciences or equivalent
  • Hands-on experience with ex vivo and in vitro liver (e.g. hepatocytes, next generation 2D and 3D fluidics models)
  • Hands-on experience in in vitro enzymology, drug transporters, drug metabolism, disposition studies
  • Hands-on experience in bioanalytical assay development (LC/MS)
  • Experience of modelling cellular processes
  • Basic knowledge and strong interest in PBPK and PK/PD are required
  • Ability to independently diagnose and design specific tailor-made study packages to tackle complex compound-specific problems
  • Strong interpersonal skills necessary for facilitating efficient interactions with both internal teams and external collaborators

Nice to have

  • Analytical Reasoning
  • Clinical Data Management
  • Clinical Pharmacology
  • Clinical Trials Operations
  • Coaching
  • Critical Thinking
  • Drug Discovery Development
  • Empowering People
  • Pharmacokinetic Modeling
  • Pharmacokinetics
  • Pharmacology
  • Pharmacometrics
  • Program Management
  • Report Writing
  • Scientific Research
  • Technologically Savvy

What the JD emphasized

  • PhD
  • Hands-on experience with ex vivo and in vitro liver (e.g. hepatocytes, next generation 2D and 3D fluidics models)
  • Hands-on experience in in vitro enzymology, drug transporters, drug metabolism, disposition studies
  • Hands-on experience in bioanalytical assay development (LC/MS)
  • Basic knowledge and strong interest in PBPK and PK/PD are required