Clinical Development Medical Director- Hepatology
Boston, Suffolk County, Massachusetts, 02298, USA
Listed on 2026-08-04
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Science
Clinical Research
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. The location of this role will therefore subsequently change to Cambridge in accordance with timelines to be set by the Company. The relocation is currently proposed to take effect by early 2029.
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.
We are seeking an experienced Medical Director for the role of Medical Director Clinical Development
- Hepatology within GSK's Respiratory, Immunology & Inflammation Research Unit. If appointed to this role you will have key responsibility for the identification of next generation targets for liver disease and the progression of assets directed towards them into the clinic to demonstrate proof of concept. To do this you will provide medical and scientific expertise and leadership to clinical and translational studies at, and above, asset‑level;
contribute to assessment of the therapeutic potential of novel mechanisms and targets, collaborate in the design of target validation programs, identify and drive life‑cycle expansion and innovative clinical development opportunities. You will work cross‑functionally to develop and execute clinical development plans (CDPs) and contribute to above‑project development of foundational and real‑world data, and translational and biomarker capabilities, within a department that prioritizes understanding mechanism and unmet need alongside innovative clinical development, helping us deliver differentiated medicines that change the course of disease and improve patients' lives.
In the Respiratory, Immunology, and Inflammation Research Unit (RIIRU), our enduring purpose is to leverage science to identify novel treatments to address underlying organ dysfunction and disease. We are trailblazing a pipeline of medicines to dramatically improve how we cure and care for patients. We are a diverse team of industry‑leading experts who channel our passion for scientific exploration into true value for patients and GSK.
We drive the end‑to‑end R&D journey, fueling early discovery and our mid‑stage pipeline while also advancing our late‑stage medicines to launch. We are combining field‑leading data sets, capabilities and methods with decades of knowledge, to transform our success in how we innovate new medicines.
This role is hybrid. You will be on‑site at one of the posted locations at least two days per week. Remote work is available on other days.
Position Summary:This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
Clinical Development Strategy and Study & Program Design- Provide effective support and oversight of R&D evidence generation strategy, plan and activities to ensure patient safety and on‑time, in‑full study delivery. Contribute to the study team discussions on indication planning and incorporate input from across disciplines (scientific, clinical, commercial, regulatory, stats, etc.) to contribute to vital deliverables including early medicine profile, target validation, translational plans, candidate selection.
- Design clinical development plans, study protocols and associated documents across all phases of development, reflecting internal and external stakeholder input (e.g., patients, evidence generation, regulators, payors, pharmacovigilance).
- Bring clinical expertise to regulatory interactions and documents including briefing documents, presentations, addressing questions and…
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