Skip to content
Updated How AI-exposed are the skills employers are hiring for? See the data →

From the employer's careers site First seen 27 Oct 2026

Director, Quantitative Systems Pharmacology

GSK Stevenage Hybrid senior full-time

Salary

$188,100 to $313,500 per year

Apply on GSK

Description

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives.

The Department of Clinical Pharmacology and Quantitative Medicine (CPQM) in the GSK Respiratory, Immunology and Inflammation Research Unit is recruiting for a Quantitative Systems Pharmacologist Lead. You will play a critical role in the day-to-day driving integration of end-to-end model-informed drug discovery and development through building and applying mechanistic QSP and QST models.

Main responsibilities and accountabilities also include:

  • Build and/or guide mathematical model development to understand disease, its progression, and drug action to prevent, treat and cure diseases; conduct simulations to assess trial design performance
  • Apply mechanistic models of biological, physiological, and pathophysiological processes to evaluate a disease, its pathways and progression, as well as drug candidates or treatment modalities
  • Develop and/or utilize state-of-the-art mathematical tools including knowledge of inverse-problem modelling and simulation, scientific ML and/or statistical techniques to gain insight into causal relationships between individual components of system-level and drug-level responses of drug-target-biomarker-disease-patient interaction
  • Define and execute a coordinated scientific and technical strategy (3-24 months planning horizon) with demonstrated ability to co-ordinate outputs from several expertise areas to determine strategy
  • Work in close collaboration with biologists, clinicians, clinical pharmacologists, pharmacometricians, statisticians, AIML, imaging, biomarker and other partner line colleagues to inform research and development programs and improve our understanding of disease mechanisms
  • Implement best practices, trends, lessons learned from internal and external sources to further clinical pharmacology modelling and simulation contributions to R&D pipeline
  • Create a collaboration framework with internal and external experts in the development and application of these models
  • Learn and apply emerging modeling and simulation methodologies with a view to enhance clinical program efficiency and investment decision quality; collaborate with external field-leading teams for methodology application
  • Able to efficiently and effectively interact with line and middle management, staff and external contacts on a functional, strategic and tactical level
  • Represent QSP CPQM on various internal advisory boards, companywide initiatives and/or leadership teams
  • Promote transparency and communicate R&D achievements through publications in appropriate scientific journals

Basic Qualifications:

  • PhD, MD, or PharmD with experience in mechanistic modelling and simulation and systems biology with applications in pharmaceutical research and development
  • Minimum 7 years of experience in mechanistic mathematical modeling, inverse problem modeling and simulation, and/or scientific machine learning methodologies to be applied to pre-clinical and/or clinical questions in drug development to solve practical problems in the pharmaceutical industry
  • Experience working with senior stakeholders in a cross functional environment
  • Track record of implementation of Model-Informed Drug Discovery and Development (MIDD) approaches to accelerate patient access to novel therapies and to expand therapeutic indications of marketed drugs

Preferred Qualifications:

  • Strong drive and agility to quickly learn and build knowledge on a drug-disease system, the mechanism, endpoints, progression, prevention, treatments, and trial design
  • Demonstrated aptitude for productive collaboration in a multi-discipline team, using effective communication and taking personal accountability for timely delivery of results
  • Clear evidence / experience in making sound judgement in complex situations and adapting to changing business needs by prioritizing multiple tasks
  • Prior experience in Hepatology, Respiratory and/or Cardiometabolic diseases is a plus

Skills

Required

  • Drug Design
  • Drug Development
  • Drug Discovery Process
  • Medication Safety
  • Molecular Modeling
  • Pharmaceutical Regulatory Compliance
  • Pharmaceutical Sciences
  • Pharmacodynamics
  • Pharmacokinetics
  • Pharmacology
  • Pharmacometrics
  • Pharmacovigilance
  • Study Design
  • Target Validation
Apply on GSK