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Director, Quantitative Clinical Pharmacology
Director, Quantitative Clinical Pharmacology-October 2024
Chicago
Oct 22, 2026
About Director, Quantitative Clinical Pharmacology

  Site Name: USA - Pennsylvania - Upper Providence, USA - Florida - Tampa, USA - Georgia - Atlanta, USA - Illinois - Chicago, USA - Maryland - Baltimore, USA - New York - Albany, USA - New York - Buffalo, USA - Ohio - Cleveland, USA - Ohio - Columbus , USA - Pennsylvania - Pittsburgh, USA - Texas - Dallas, USA - Texas - Houston, Washington DC

  Posted Date: Nov 14 2023

  The Department of Clinical Pharmacology Modeling and Simulation (CPMS) at GlaxoSmithKline (GSK) is recruiting for a Director-level quantitative clinical pharmacologist. Locations include Collegeville, PA, Durham, NC, Cambridge, MA in the U.S. or Stevenage in the U.K.. Remote working may be considered for the right candidate.

  This position represents a key opportunity for professionals with PhD, MD, PharmD or equivalent doctoral background, who are experienced clinical pharmacologists and pharmacometricians to advance the vision and mission of GSK's rapidly expanding Infectious Disease portfolio including vaccines to prevent, treat and cure infectious diseases. Sought after experiences for this position include building and integrating mechanistic mathematical models and disease platforms with advanced analytical techniques (such as machine learning) to enhance the robustness and quality of decision-making from exploratory research, clinical development, registration and life cycle management.

  You will be expected to play a critical role in driving integration of end-to-end model-informed drug discovery and development. In addition, you will be accountable to define, coordinate and defend Clinical Pharmacology Modelling & Simulation development strategies for disease & therapeutics of interest at senior level meetings, and provide expert input into the clinical pharmacology evidence generation and integrated evidence plans. CPMS responsibilities and accountabilities generally commence at candidate selection with preparations of first time in human trials, and continue through to filing, registration, and market expansion.

   Main responsibilities and accountabilities also include: Establish or guide mathematical model development to understand disease, its progression, and drug action to prevent, treat and cure diseases; conduct meta-analyses as appropriate to generate knowledge through data re-use; conduct simulations to assess trial design performanceDefine and execute a co-ordinated scientific and technical strategy (18-24 months planning horizon) with demonstrated ability to co-ordinate outputs from several expertise areas to determine strategyBuild and utilize mechanistic models of biological, physiological, and pathophysiological processes to evaluate a disease, its pathways and progression, as well as drug candidates or treatment modalitiesWork in close collaboration with bench biologists, data scientists, computational biologists, clinicians and other partner line colleagues to inform research and development programs and improve our understanding of disease mechanismsDevelop and/or utilize state-of-the-art mathematical tools to gain insight into causal relationships between individual components of system-level and drug-level responses of drug-target-biomarker-disease-patient interactionCreate a collaboration framework with internal and external experts in the development and application of these modelsLearn 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 applicationImplement best practices, trends, lessons learned from internal and external sources to further clinical pharmacology modelling and simulation contributions to R&D pipelineAbility to interact with line and middle management, staff and external contacts on a functional, strategic and tactical levelRepresent CPMS on various internal advisory boards, companywide initiatives and/or leadership teamsPromote transparency and communicate R&D achievements through publications in appropriate scientific journals Why you?

  Basic Qualifications:

  We are looking for a professional with these required skills to achieve our goals:PhD, MD, or PharmD with experience in clinical pharmacology, modelling and simulation in pharmaceutical research and developmentFive or more years of experience in mechanistic mathematical modeling to apply to clinical questions in drug developmentFive or more years of experience in clinical pharmacokinetics, modelling/simulation and drug development to solve practical problems in pharmaceutical industryPreferred Qualifications:Strong drive and learning agility to build knowledge on a drug-disease system, symptom progression, standard of care, and trial designDemonstrated aptitude for productive collaboration in a multi-discipline team, using effective communication and taking personal accountability for timely delivery of resultsClear evidence of ability to make sound judgement in complex situations and adapt to changing business needs by prioritizing multiple tasksExperience working with senior stakeholders in a cross functional environmentStrong 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 Why GSK?

  We're combining the power of genetic and genomic insights into what causes disease, with the speed and scale of artificial intelligence and machine learning (AI/ML) to make better predictions about who a treatment might work for, and why. We believe this powerful combination of data and technology holds the key to fundamentally transforming medical discovery for the better, improving R&D success rates and shaping how even the most challenging diseases, like neurological conditions and cancer, can be both prevented and treated.

  In 2021 we delivered four major product approvals: Cabenuva for HIV, Jemperli for endometrial cancer, Xevudy for COVID-19 and Apretude , our new long-acting medicine for HIV prevention.

  #LI-GSK

  Please visit GSK US Benefits Summary t o learn more about the comprehensive benefits program GSK offers US employees.

  Why Us?

  GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organization where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.

  Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.

  If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).

  GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

  Important notice to Employment businesses/ Agencies

  GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

  Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site.

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Director, Quantitative Clinical Pharmacology
Site Name: USA - Pennsylvania - Upper Providence, USA - Florida - Tampa, USA - Georgia - Atlanta, USA - Illinois - Chicago, USA - Maryland - Baltimore, USA - New York - Albany, USA - New York - Buffa
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