Senior Director, Hepatology Translational Biology

GlaxoSmithKline

Upper Providence (Delaware County)

On-site

USD 226,000 - 377,000

Full time

3 days ago
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Benefits offered by this job

Annual bonus
Healthcare
Pension plan
Shares and savings programme

Job summary

GlaxoSmithKline is seeking a Senior Director in Translational Biology for Hepatology to shape strategy and lead preclinical to clinical translation. You will work across discovery and translational science to de-risk clinical development and drive biomarker strategies, with strong influence across the hepatology portfolio.

The role offers significant leadership within an established hepatology program, opportunities for external collaborations, and a path to impact patient outcomes through

Qualifications

  • MD/PhD or PhD with extensive experience in preclinical biology and translational strategies in liver disease.
  • Experience leading hepatology programs and translating human biology to clinical development.
  • Ability to influence decisions in a matrix environment through data-driven recommendations.

Responsibilities

  • Provide scientific leadership across discovery and early clinical hepatology programs (MASH, ALD) and related comorbidities.
  • Define translational plans, target validation strategies, and biomarker development for clinical success.
  • Lead external collaborations and diligence for business development opportunities.
  • Drive portfolio recommendations and strategic alignment across discovery and development.
  • Mentor teams and ensure high scientific standards and reproducibility.

Skills

Preclinical biology
Translational biology
Hepatology
Matrix leadership
Data-driven decisions

Education

MD/PhD or PhD in cell or molecular biology, genetics, pharmacology, hepatology or related discipline

Job description

We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.

We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.

Discover more about our company wide benefits and life at GSK on our webpage Life at GSK | GSK

Senior Director, Hepatology Translational Biology

In the Respiratory, Immunology and Inflammation Research Unit (RIIRU), we combine deep scientific expertise, leading datasets and innovative technologies to discover and develop medicines that address underlying organ dysfunction and disease. Our teams work across the R&D lifecycle, from early discovery through clinical development and launch, with a shared ambition to deliver meaningful outcomes for patients.

We are seeking an experienced Senior Director to join the Translational Biology Unit and provide scientific leadership for our hepatology portfolio. Reporting to the Head of Hepatology Translational Biology, this senior individual contributor will bring deep expertise in preclinical biology and forward and reverse translation, shaping strategy and advancing programmes in MASH, ALD and associated cardiometabolic co‑morbidities, including cardiovascular disease and obesity. Working across the RIIRU hepatology matrix, you will connect human disease biology with target science, biomarkers and clinical development, ensuring strong human relevance of preclinical evidence and helping to de‑risk translation into the clinic. You will also shape high‑impact academic collaborations and provide scientific leadership for business development opportunities that strengthen and accelerate the portfolio.

The role offers significant influence across an established and diverse hepatology portfolio spanning clinical‑stage programmes, preclinical projects and target identification. As a key leader within the Hepatology Disease Area Acceleration Team, you will help align patient biology, target hypotheses, translational strategies, biomarkers and clinical endpoints across discovery and development. Working closely with Translational Biology, disease‑area biology, Clinical and Translational Sciences and senior portfolio leaders, you will use human data and reverse translation to guide evidence‑based decisions and advance differentiated medicines with meaningful potential for patients.

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.

In this role you will
Scientific and Translational Leadership (Individual Contributor)
  • Provide scientific leadership across a portfolio of discovery and clinical‑stage hepatology programs focused on MASH, ALD, and more broadly liver disease with cardiometabolic comorbidities.
  • Define and drive human‑relevant mechanistic hypotheses, target validation strategies, and translational plans that strengthen confidence in clinical success.
  • Partner with Research & Development Technologies, Translational Sciences, and disease‑area experts to identify, validate, and advance novel therapeutic opportunities.
  • Lead development of biomarker strategies spanning target engagement, pharmacodynamics, disease activity, patient stratification, and clinical decision‑making.
  • Anticipate emerging scientific and competitive trends and translate insights into evidence based portfolio recommendations.
Matrix Leadership and Strategic Influence
  • Influence scientific direction and decision‑making across cross‑functional teams through data driven leadership and expert judgment.
  • Align stakeholders around key experiments, success criteria, translational strategies, and portfolio priorities.
  • Ensure rigorous scientific standards, reproducibility, and fit‑for‑purpose model selection across discovery and translational research activities.
  • Provide mentorship and scientific guidance to project teams and colleagues across the matrix.
Cross‑Functional Collaboration
  • Partner closely with biology, clinical development, translational medicine, biostatistics, DMPK, pathology, safety, and platform teams to deliver integrated development strategies.
  • Translate complex preclinical and clinical datasets into actionable insights that inform target selection, patient stratification, and study design.
  • Drive efficient target progression and support clinical programs through integrated translational plans.
Innovation and External Engagement
  • Champion innovative approaches, technologies, and model systems that enhance portfolio differentiation and translational success.
  • Establish and lead strategic collaborations with academic institutions, CROs, biotechnology companies, and key opinion leaders.
  • Build and maintain a network of external experts to access emerging science, novel technologies, and unique research capabilities.
Business Development
  • Contribute scientific leadership to evaluation and diligence activities for external opportunities.
  • Assess target biology, translational evidence, competitive differentiation, and portfolio fit to support investment decisions.
Quality, Compliance and Resource Stewardship
  • Ensure research activities are conducted in compliance with applicable policies, ethical standards, and quality expectations.
  • Help optimize portfolio investments by prioritizing critical‑path activities and recommending effective deployment of internal and external resources.
Why you?
Basic Qualifications & Skills:

We are looking for professionals with these required skills to achieve our goals:

  • MD/PhD or PhD in cell or molecular biology, genetics, pharmacology, hepatology or a related discipline with extensive experience in preclinical biology and forward and reverse translation in liver disease.
  • Extensive experience in the pharmaceutical/biotechnology industry, with a focus on hepatology therapeutics (MASH and ALD) and a strong understanding of target mechanisms and translational evidence needed to support early clinical development.
  • Demonstrated ability to operate as a senior individual contributor and scientific thought leader, influencing decisions in a matrix environment through data‑driven recommendations, clear communication, and strong collaboration.
  • Experience leading and managing external collaborations and diligence of business development opportunities.
  • Proven track record of advancing targets and/or assets through key discovery and early development milestones, including development of fit‑for‑purpose translational packages (e.g., mechanistic rationale, human relevance, biomarker strategy, and clinical hypothesis support).
  • Strong knowledge of hepatology disease biology (MASH and ALD), pathways and mechanisms, and an appreciation of relevant co‑morbidities (e.g., cardiovascular disease and obesity) that shape patient biology, endpoints, and clinical development strategy
Preferred Qualifications & Skills:

Please note the following skills are not necessary, just preferred, if you do not have them, please still apply:

  • Demonstrated strength as a translational scientist who can work with the Hepatology Disease Area Acceleration Team, the Hepatology Clinical Research Head, and aligned Early Development and Medicine Development Leaders to interpret complex data and external trends; connect preclinical findings to clinical endpoints; and provide scientific recommendations on indication expansion, patient stratification, biomarker strategy, and potential business development opportunities (including assets spanning cardiometabolic comorbidities).
  • Strong business acumen and understanding of commercial aspects, including marketing, sales, and market access.
  • Excellent communication and presentation skills, with the ability to effectively engage with internal and external stakeholders.
  • Demonstrated ability to work in a fast‑paced, dynamic environment and manage multiple priorities.
  • Knowledge of regulatory requirements and compliance standards in the pharmaceutical industry.
Working environment and travel

This role sits in an established but evolving portfolio and requires a leader who can add deep expertise immediately, while working collaboratively across shared resources and governance. The successful candidate will combine scientific authority with humility, clear communication and a strong bias towards action. Travel is expected to be reasonable and purposeful, including scientific conferences and occasional international collaboration meetings.

Closing Date for Applications - Sunday 15th November

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

Skills

Biotechnology, Business Strategies, Cell Biology, Cross‑Functional Teamwork, Drug Development, Drug Discovery Process, Influencing Without Authority, Interpersonal Communication, Life Science, Market Opportunities, Matrix Leadership, Molecular Biology, Scientific Research, Scientific Writing, Strategic Alignment* 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 $226,050 to $376,750. 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. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.

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

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.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at usrecruitment.adjustments@gsk.com.

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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