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In Vivo Respiratory Principal Scientist

GSK
Full-time
Remote friendly (Collegeville, PA)
United States
Clinical Research and Development

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Role Summary

In Vivo Respiratory Principal Scientist leading design, execution, and reporting of preclinical integrative in vivo/in vitro/ex vivo experiments to support therapeutic area teams and drug discovery projects from target validation through to clinical phases in the respiratory disease area.

Responsibilities

  • Contribute to the design and lab/vivarium-based execution of in vivo strategies for the respiratory disease area.
  • Contribute to the delivery of Respiratory preclinical efficacy and mechanistic in vivo studies using respiratory models to enable PK/PD and translational biomarker data generation.
  • Lead discussions to define rationale, objectives, endpoints, and Go/No-Go decisions for in vivo models, setting goals and timelines.
  • Design, execute, analyze, and present in vivo studies as the In Vivo Leader (IVL) on portfolio projects with input from Biology Leader, Project Leader, and Complex Models Leadership Team.
  • Apply robust study design principles, obtain input from SMEs and matrix partners prior to endorsements for animal studies.
  • Resolve technical challenges in experimental planning, setup and execution with minimal guidance.
  • Conduct lab/vivarium-based execution to enable sample/tissue acquisition and analysis, integrating PK/PD and translational biomarker data; utilize ex vivo assays as needed (flow cytometry, ELISAs, MSD, Luminex, qPCR).
  • Serve as key contact for animal studies, including out-of-hours procedures as required.
  • Maintain technical expertise in animal handling, dosing, blood and tissue collection, and measurements of lung function and hemodynamics.
  • Be familiar with federal laws governing animal use and local governance processes (IACUC, AUP); adhere to welfare and treatment guidelines.
  • Assess animal health and welfare, document findings, and act or seek expert advice when necessary.
  • Collaborate effectively with internal matrix partners and external studies (CROs, academic groups) as study monitor.
  • Lead external animal studies and monitor studies; maintain accurate electronic lab records compliant with data integrity standards.
  • Foster a culture of innovation, collaboration, inclusion, and continuous learning; stay current with literature and apply to in vivo strategies.

Qualifications

  • BSc in biological science with 5+ years of respiratory in vivo experience, or MSc with 4+ years, or PhD with 2+ years in industry or academia.
  • Knowledge of COPD and IPF/ILD mechanisms and use of in vivo systems to interrogate pathophysiology.
  • Hands-on experience with respiratory animal model systems including lung function measurements (e.g., whole-body plethysmography, dynamic compliance/resistance, FEV/FVC).
  • Experience with in vivo dosing (intranasal, intratracheal), tissue necropsy (BAL and lung dissection), and blood sampling.
  • Experience with Flow Cytometry, ELISAs, MSD, Luminex, and qPCR or RNAseq.
  • Experience supervising external animal studies as a study monitor.
  • Experience writing and critiquing scientific documents and communicating findings clearly to line and matrix teams.

Preferred Qualifications

  • Biomarker assay development expertise in respiratory disease to define PK/PD parameters and inform translational research.
  • Experience in drug discovery processes and knowledge of drug discovery pillars.
  • Familiarity with omics platforms (spatial, bulk and single-cell RNA-seq) and advanced imaging technologies.
  • Ability to balance multiple priorities and meet deadlines.
  • Knowledge of regulatory guidelines relating to animal use and compliance requirements.