The Principal Scientist role involves working with the Genomic Technologies team to analyze large-scale genetic data, identify causal gene-phenotype links, and develop methods for genetic and genomic data analysis. The role requires expertise in statistical genetics, programming skills in R or Python, and experience with large biobank datasets.
The Principal Scientist role in Genomic Technologies at GSK involves integrating deep expertise in computational and statistical methods to analyze large-scale genetic and genomic data. Responsibilities include developing and improving methods for genetic data analysis, collaborating with multidisciplinary teams, and contributing to drug discovery and development projects.
This role involves designing and executing biochemical and molecular biology assays to support pharmacokinetic/pharmacodynamic analysis. Responsibilities include developing robust mRNA-based bioanalytical capabilities, troubleshooting scientific issues, and collaborating with external partners. The position also offers opportunities to work with Generative AI and digital tools to enhance scientific workflows.
This role involves providing engineering support for GMP manufacturing equipment, ensuring operability and reliability across process platforms. Responsibilities include troubleshooting, authoring technical documents, and leading small-to-medium sized projects. The position is hands-on and cross-functional, essential for mRNA manufacturing success.
A Research Scientist in Machine Learning will develop novel deep learning models and algorithms to advance drug discovery at digital speed. Working in an interdisciplinary environment, they will apply cutting-edge ML techniques to complex biological and chemical problems, iterating closely with domain experts. The role involves leading high-ambition research projects, scaling training frameworks, and shaping the technical direction of AI-driven drug design.
Lead the development and execution of bioanalytical strategies for a diverse portfolio of AI-designed therapeutics, including small molecules, biologics, and ADCs. Design and validate PK, PD, and immunogenicity assays, manage global CROs, and integrate bioanalytical data into AI models to refine drug discovery. Play a key role in IND-enabling studies and cross-functional preclinical development in a hybrid London-based role.
This role involves conducting high-impact research in plant specialised metabolism engineering, focusing on the development of novel decarbonised plant-based production of food and medicines. The scientist will work in a collaborative environment, designing and conducting experiments, developing customized libraries, and driving the translation of research into real-world solutions.
This role involves designing and optimizing high-throughput, image-based phenotypic screening workflows for plant cells, developing robust imaging assays, and collaborating with automation and AI teams to integrate scalable screening processes. The scientist will work on cutting-edge research to enhance plant productivity and sustainability, contributing to publications and IP generation.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, and collaboration with cross-functional teams to ensure patient safety and clinical integrity.
This role involves providing medical leadership within oncology clinical development, specifically in genitourinary (GU) cancers. The Medical Director will lead medical monitoring, ensure patient safety, contribute to study design and regulatory interactions, and interpret clinical data to inform decision-making. They will work closely with cross-functional teams and external experts to advance GSK’s oncology pipeline with a focus on high unmet need areas.
This role involves leading medical oversight and clinical strategy for genitourinary (GU) oncology trials within GSK’s R&D pipeline. The Medical Director provides physician-level expertise in study design, safety monitoring, data interpretation, and regulatory engagement, ensuring patient safety and scientific integrity. They collaborate with cross-functional teams and external experts to advance innovative cancer treatments through clinical development.
This role involves leading medical strategy and oversight for genitourinary (GU) oncology clinical trials within GSK’s R&D pipeline. The Medical Director provides physician-level expertise in study design, real-time safety monitoring, data interpretation, and regulatory engagement, ensuring patient safety and clinical integrity. They work cross-functionally within a matrix team to advance innovative cancer therapies from development through to regulatory submission and scientific dissemination.
This role involves providing medical leadership within oncology clinical development for genitourinary (GU) cancers, focusing on study design, medical monitoring, and safety oversight. The physician will interpret clinical and safety data, contribute to regulatory submissions, and engage with investigators and external experts. Working within a cross-functional team, the role ensures patient safety and clinical integrity across trials while supporting GSK’s mission to advance innovative cancer treatments.
This role involves providing medical leadership in oncology clinical development for genitourinary (GU) cancers, with responsibility for medical monitoring, safety oversight, and clinical data interpretation across trials. The Medical Director integrates physician expertise into study design, regulatory interactions, and cross-functional decision-making, working within a global matrix team. The position requires deep oncology knowledge, experience in clinical trial conduct, and strong collaboration with internal teams and external experts.
This role involves providing medical leadership in oncology clinical development, specifically for genitourinary (GU) cancers. The Medical Director will lead medical monitoring, contribute to protocol design, interpret clinical data, and ensure patient safety across clinical trials. They will work closely with cross-functional teams, engage with external experts, and support regulatory submissions and scientific communications within a global pharmaceutical environment.
