Associate Director, PBPK-PD Translational Modeling, DMPK

Associate Director, PBPK-PD Translational Modeling, DMPK

Drug Metabolism and Pharmacokinetics (DMPK) | Research & Development GSK.

Closing Date: 1st September 2026 (COB)

Business Introduction
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. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success.

We're uniting science, technology, and talent to get ahead of disease together.
Find out more:
Our approach to R&D

For candidates seeking to be located at our Stevenage site, this role will temporarily be based ever, the Company plans to relocate its offices to Cambridge, UK. The location of this role will therefore subsequently change to Cambridge, UK in accordance with timelines to be set by the Company. The relocation is currently proposed to take effect by early 2029.

Position Summary

We have an exciting opportunity for a scientifically ambitious Associate Director to join the PBPK-PD Translational Modeling group within DMPK. The role focuses on developing and applying mechanistic PBPK-PD models for oligonucleotide therapeutics and antibody-drug conjugates, translating in vitro and preclinical data into predictions of tissue exposure, target engagement, and pharmacological effects in patients. Experience in T-cell and myeloid cell engager modelling is advantageous.

You will provide PBPK-PD expertise to support target validation, modality selection, human dose prediction, and PK/PD strategies from early discovery through first-in-human studies. The role also involves integrating PBPK-PD, QSP, and AI-enabled modelling approaches to drive data-informed candidate selection and development decisions

Working arrangement

This role is offered on a hybrid basis (UK or US), with an expectation of typically 2 to 3 days per week on-site and flexibility according to business needs and local policy.

Responsibilities

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

Translational PBPK-PD modeling for Biologic Modalities

• Building, qualifying and applying mechanistic whole-body PBPK-PD models for siRNA, ASO and conjugated oligonucleotides
• Building and applying ADC PBPK models integrating antibody disposition, target expression and internalization, DAR distribution and deconjugation, linker stability, payload release and intratumoral penetration including bystander effects
• Delivering human efficacious dose projections - translating preclinical PK/PD into clinical dose, regimen and duration with explicit treatment of uncertainty and driving assumptions
• Defining project-level PK/PD modeling strategies and articulating them to project teams and governance bodies
• Creating opportunities to apply integrated PBPK-PD and QSP approaches earlier in discovery
• Partnering with Discovery, Biology, Chemistry, Toxicology, Bioanalysis and Clinical Pharmacology to embed model-informed drug discovery and development (MID3) into the standard progression path and define quantitative candidate selection criteria
• Applying AI/Tech-enabled modeling frameworks is essential to this role
• Engaging line and middle management, project teams and external partners at functional, strategic and tactical level, and representing DMPK modeling at internal forums and project team meetings
• Promoting external credibility through peer-reviewed publications and conference presentations.

Why You?

Basic Qualifications

We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

• PhD in pharmacokinetics, pharmaceutical sciences, chemical or biomedical engineering, systems pharmacology, applied mathematics, statistics or a closely related quantitative discipline.
• Strong experience developing and applying mechanistic PBPK and/or PK-PD models in an industry or equivalent research setting, with verifiable proficiency in PBPK and systems modeling platforms (e.g. Simcyp, Sim Biology/MATLAB, etc.).
• Demonstrated experience delivering human PK and efficacious dose predictions and translational PK/PD assessments.
• Demonstrated ability to apply AI/Tech-enabled modeling frameworks

Preferred Qualifications

If you have the following characteristics, it would be a plus:

• Direct experience modeling oligonucleotide and antibody-drug conjugates or other bioconjugates
• Track record of implementing MID3 approaches to accelerate progression of novel therapeutics and to strengthen the quality of portfolio decisions
• Demonstrated aptitude for productive collaboration in a multi-disciplinary matrix team, with effective communication and…