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Principal Research Scientist - Modeling and Simulation

AbbVie
Full-time
On-site
Irvine, CA
$121,000 - $230,000 USD yearly
Clinical Research and Development

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Role Summary

Principal Research Scientist โ€šร„รฌ Modeling and Simulation is an onsite role based out of Irvine, CA. The role contributes pharmacokinetic and modeling and simulation expertise to build in silico drug models describing exposureโ€šร„รฌresponse relationships to support formulation development and early-stage clinical development, across non-clinical models and humans. The role involves exploratory analyses and non-conventional modeling, with a focus on ophthalmology and aesthetics/dermatology, in a fast-paced, independent environment.

Responsibilities

  • Apply PK and PK/PD modeling/simulation to guide the design and execution of in vivo preclinical animal experiments and/or early-stage clinical trials.
  • Identify opportunities to apply and develop modeling and simulation strategies across the R&D portfolio, with a focus on ophthalmology and aesthetics/dermatology.
  • Integrate M&S knowledge to contribute to optimizing translational sciences strategies.
  • Analyze PK/PD data, clinical and nonclinical, using advanced modeling to support dose selection, study design, and proof-of-concept.
  • Identify and monitor vendors/consultants or engage internal resources to meet project deliverables.
  • Collaborate with stakeholders to conduct and integrate data analyses and summarize modeling outcomes to support IND, CTA, IMPD, NDA, and BLA filings and regulatory communications.
  • Engage in exploratory analyses and non-conventional modeling beyond systemic drug development with a focus on locally-administered/acting products.
  • Maintain awareness of current technologies in PK/PD and PBPK modeling.
  • Develop partnerships with nonclinical/clinical pharmacology/PKPD, biomarker scientists, safety scientists, researchers, clinicians, and project teams.
  • Design and oversee preclinical PK/TK studies.
  • Establish collaborations to facilitate data integration for biomarker selection, candidate nomination/selection, and human dose prediction.

Qualifications

  • BS with typically 14+ years of experience OR MS with typically 12+ years of experience OR PhD with typically 6+ years of experience in Pharmaceutical Sciences, Quantitative Pharmacology, Biomedical/Chemical Engineering, Pharmacometrics or related field
  • 2+ years of experience in PK/PD modeling & simulation, quantitative pharmacology, and/or applied population PK in the pharmaceutical industry
  • Academic and/or industry experience in PBPK modeling or population PK/PKPD modeling
  • Strong knowledge of biology (mechanism of action)/pharmacology, clinical immunology, protein sciences, statistics, and pharmaceutical development
  • Ability to learn new areas of biological sciences and build on quantitative skills to develop models
  • Data manipulation and programming skills with SAS, R, S+ or similar; experience using Phoenix WNL, GastroPlus, and SimCyp
  • Scientific publications in area of specialization
  • Effective written and verbal communication skills
  • Strong collaboration skills
  • Ability to stay up-to-date with scientific and technological developments in modeling
  • Ability to work within a diverse workforce

Preferred Experience

  • Experience with biologics including gene therapy
  • Experience with programming and data analysis tools/languages such as R, Matlab, Berkeley Madonna, ADAPT
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