Director, Quantitative Clinical Pharmacologist

Upper Providence, GSK HQ, Stevenage, Waltham

Posted date: Jan 6 2026

GSK has an inspiring ambition: by uniting science, technology and talent we aim to positively impact the health of 2.5 billion people over the next ten years. We will get ahead of disease together with our R&D approach of focusing on the science of the immune system, human genetics and advanced technologies such as functional genomics and AI/ML.

We have an exciting opportunity at GSK for a highly innovative Quantitative Clinical Pharmacologist to join our team supporting the infectious disease area. GSK provides a supportive environment for scientists who are aspiring to learn, contribute and make an impact on business decisions through innovation, expertise and influence.

You will be part of a science‑driven group delivering clinical pharmacology and modelling & simulation excellence to research and development programs. You’ll have the opportunity to work on both small molecules and biologics in the Vaccines and Infectious Disease therapeutic area. Responsibilities commence post‑candidate selection with accountability beginning approximately 6 months prior to FTIH through to life cycle management.

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• Contribute, as a member of a multi‑disciplinary team, to the design of an efficient clinical development program, robust registration package and support life cycle management of an asset.
  
• Provide optimal application of Clinical Pharmacokinetic (PK), Pharmacodynamic (PD), and Modeling & Simulation (MS) principles toward efficient drug development, risk management, and registration of compounds.
  
• Play a central role in predicting human dose range, characterizing exposure‑response relationships and justifying dose recommendations for special populations.
  
• Develop mathematical models to understand disease progression and drug pharmacodynamics and pharmacokinetics; conduct meta‑analyses to generate knowledge through data re‑use; conduct simulations to assess trial design performance.
  
• Present strategy and discuss outcomes of model‑based approaches via interactions with governance boards and regulatory agencies.
  
• Provide a thorough understanding and ability to apply appropriate FDA and ICH guidelines in the design of clinical studies and drug development strategy.
  
• Promote model‑informed drug discovery and development (MID3) through external collaboration, journal publication and conference presentation.
  
• Design and interpret clinical pharmacology studies to evaluate potential effects of intrinsic and extrinsic factors on pharmacokinetics and pharmacodynamics.
  
• Identify opportunities to utilize in silico PBPK approaches to replace in‑vivo clinical studies to explore the impact of DDI and special populations on PK where appropriate.
  
• Write sections of drug development and registration documents such as clinical trial protocols and reports, clinical investigator brochures and regulatory submission packages.
  
• Learn and apply emerging modelling and simulation methodologies with a view to enhance clinical program efficiency and investment decision quality; collaborate with external field‑leading teams for methodology application.
  
• Innovate through working effectively with colleagues in the department and other matrix team members, including statisticians, biologists, physicians and drug metabolism scientists.
  

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• Advanced Degree in Life science such as PhD, PharmD or MD to enable a successful career in quantitative clinical pharmacology in pharmaceutical research and development.
  
• 5+ years experience in clinical pharmacokinetics, modelling & simulation and model‑informed drug development including designing, analysing and reporting clinical studies.
  
• 2+ years experience of pharmacokinetic and pharmacodynamic principles and commonly applied models through previous projects in pharmaceutical industry roles or equivalent.
  
• 2+ years experience working with common tools for quantitative clinical pharmacology such as NONMEM, R, WINNONLIN, SIMCYP, SAS and MATLAB through previous hands‑on projects.
  
• 1+ year experience with regulatory submission documents such as CTAs, INDs, NDAs, MAAs and BLAs through direct involvement in regulatory submission activities in previous roles.
  
• 1+ year experience applying appropriate FDA and ICH guidelines in the design of clinical development plans and studies.
  

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• Knowledge of or ability to quickly learn the mechanism, endpoints, progression and treatments of diseases in infectious disease and other relevant therapy areas.
  
• Ability to communicate clearly and succinctly with the audience in mind, both orally and in writing.
  
• Ability to build effective collaboration while taking personal accountability for delivery of quantitative clinical pharmacology results.
  
• Sound judgement, analytical mindset and problem‑solving skills.
  
• Ability to effectively multi‑task and deliver results on time.
  

#Hybrid*
If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $180,675 to $301,125. The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share‑based long‑term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at where you can also request a call. Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

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