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Director Dmpk Jobs (NOW HIRING)

... director-level equivalent) to contribute to our company drug discovery and early clinical ... The ideal candidate will lead drug metabolism and pharmacokinetic (DMPK) efforts across multiple ...

Scientist II, Discovery DMPK Salary Range: $55,000-$65,000 Location: Exton, PA (onsite) About ... Serve as a Principal Investigator (PI) or Study Director (SD) within areas of expertise, as ...

Scientist II, Discovery DMPK

Exton, PA · On-site

$55K - $65K/yr

Scientist II, Discovery DMPK Salary Range: $55,000-$65,000 Location: Exton, PA (onsite) About ... Serve as a Principal Investigator (PI) or Study Director (SD) within areas of expertise, as ...

... DMPK and BA department. He/she will represent as a Clinical Pharmacology Lead and provide subject matter expertise on cross-functional project teams. The Clinical Pharmacology Director provides ...

Perform sample analysis for Discovery DMPK studies, including in vivo PK and in vitro ADME programs ... Serve as a Principal Investigator (PI) or Study Director (SD) within areas of expertise, as ...

Cellarity is seeking a highly strategic Sr. Director, Pharmacology to connect biology, pharmacology, DMPK, and translational science across inflammation and hematology programs. Reporting to the Sr. ...

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Director Dmpk information

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$205.5K

$246.7K

$277K

How much do director dmpk jobs pay per year?

As of Aug 31, 2026, the average yearly pay for director dmpk in the United States is $246,666.00, according to ZipRecruiter salary data. Most workers in this role earn between $230,000.00 and $261,000.00 per year, depending on experience, location, and employer.

What does a director DMPK do?

A Director of Drug Metabolism and Pharmacokinetics (DMPK) leads efforts to understand the absorption, distribution, metabolism, and excretion (ADME) of drug candidates. They design and oversee preclinical and clinical studies to optimize drug properties, ensuring efficacy and safety. This role involves collaborating with pharmacology, toxicology, and regulatory teams to drive drug development. Additionally, they interpret data, guide strategy, and contribute to regulatory submissions.

What are the key skills and qualifications needed to thrive as a director DMPK?

To thrive as a Director DMPK (Drug Metabolism and Pharmacokinetics), you need advanced expertise in pharmacokinetics, drug metabolism, and bioanalytical methods, typically supported by a PhD in pharmaceutical sciences, chemistry, or a related field. Familiarity with regulatory guidelines, data analysis platforms like WinNonlin or Phoenix, and validated laboratory systems is crucial. Strong leadership, cross-functional collaboration, and effective communication skills help in guiding multidisciplinary teams and driving complex projects forward. These capabilities ensure the development and regulatory success of new drug candidates in a highly competitive and compliant environment.

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Infographic showing various Director Dmpk job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $246,666 per year, or $118.6 per hour.

Associate Director, PBPK-PD Translational Modeling, DMPK

Collegeville, PA • Hybrid


GlaxoSmithKline
Scientific Research and Development Services • 10K+ employees

8.9

Company rating: 8.9 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

9th of 86 rated pharmaceutical

People enjoy working here

Good employer

Respectful managers


Full-time

Posted 12 days ago


Job description

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 at Stevenage. However, 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, SimBiology/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 personal accountability for timely delivery


How to apply
We welcome applicants at different stages of their careers. Please send your CV and a short cover letter describing a recent PBPK-PD or translational modelling project that had clear impact. Tell us what you modelled, the decisions you supported, and what you learned. If this role fits your skills and purpose, please apply. We look forward to hearing from you.


Skills

Artificial Intelligence (AI), Computational Sciences, Computer Programming, Data Analysis, Data Management, Data Modeling, Data Science, Predictive Modeling, Statistical Models

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

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.

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.

We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at UKRecruitment.Adjustments@gsk.com where you can also request a call.

Please note should your enquiry 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

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 the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/


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About GlaxoSmithKline

Sourced by ZipRecruiter

GlaxoSmithKline is a globally recognized pharmaceutical and healthcare company based in Philadelphia, PA, USA. Originated from a merger between Glaxo Wellcome and SmithKline Beecham in 2000, the company excels in the pharmaceutical industry and holds a leading position in making medicines, vaccines, and consumer healthcare products. GSK's mission is to improve the quality of human life by enabling people to do more, feel better, and live longer. They adhere to core values of transparency, integrity, respect for people, and patient-focus, reflecting in their endeavors to conduct research and deliver innovative healthcare solutions to patients and consumers worldwide.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Philadelphia, PA, US


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