The Medical Director, Oncology Clinical Development, focuses on lung and head/neck cancers, providing medical expertise and clinical judgement to design, conduct, and interpret clinical studies. Key responsibilities include medical monitoring, safety oversight, and collaborating with cross-functional teams to ensure patient safety and clinical integrity.
The AI Director role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to improve clinical trial outcomes. Responsibilities include leading the prioritization of AI opportunities, building and testing prototypes, and shaping deployment strategies with cross-functional teams.
This role involves designing and executing bioanalytical and immunogenicity strategies to support mRNA-based therapeutic development. The scientist will lead assay development for clinical programmes using platforms like ELISA, MSD, and cell-based methods, ensuring regulatory compliance and robust data generation. The position emphasizes collaboration across multidisciplinary teams and integration of digital tools and AI to advance Moderna's pipeline.
This role involves designing and executing bioanalytical and immunogenicity strategies to support mRNA-based clinical development programmes. The scientist will lead assay development—including ADA, nAb, PK, and PD assays—using platforms like ELISA, MSD, and cell culture, while ensuring regulatory compliance and contributing to Moderna's expanding capabilities in Harwell. The position emphasizes collaboration across multidisciplinary teams and integration of digital and AI-enabled tools to enhance data interpretation and decision-making.
A Research Scientist focused on applying Large Language Models to drug discovery, working in interdisciplinary teams to develop novel AI-driven approaches for biological and chemical challenges. The role involves advancing LLM techniques such as post-training, reasoning, tool-use, and alignment within a cutting-edge AI research environment. Collaboration with scientists and engineers is central to developing predictive models that accelerate rational drug design.
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.
The VP, Medicine Development Leader for Cancer Vaccines will lead the global development of GSK's cancer vaccine, from early stages through approval and launch. This role involves strategic planning, team leadership, and collaboration with various stakeholders across R&D and commercial functions to ensure the successful development and commercialization of the vaccine.
The VP, Medicine Development Leader for Cancer Vaccines will lead the global development of GSK's cancer vaccine, from early stages through approval and launch. This role involves strategic planning, team leadership, and collaboration with various stakeholders across R&D and commercial functions to ensure the successful development and commercialization of the vaccine.
The VP, Medicine Development Leader for Cancer Vaccines will lead the global development of GSK's cancer vaccine, from early stages through approval and launch. This role involves strategic planning, team leadership, and collaboration with various stakeholders across R&D and commercial functions to ensure the successful development and commercialization of the vaccine.
This role involves hands-on engineering support for GMP manufacturing equipment, ensuring operability and reliability across process platforms. Responsibilities include troubleshooting, project management, and continuous improvement, with a focus on mRNA manufacturing at Moderna's Harwell and Norwood facilities.
This role involves hands-on laboratory work supporting immunoassay development and clinical testing for Moderna’s mRNA-based therapeutic programs. The technician will prepare reagents, conduct sample analysis, ensure regulatory compliance, and contribute to high-quality data generation for clinical trials. Based in Oxford, the position requires full-time on-site work in a regulated lab environment with occasional overtime.
This role involves leading and executing phase-appropriate bioanalytical strategies for immunogenicity and ligand binding assays (LBA) within Moderna’s mRNA-LNP therapeutic pipeline. The Principal Scientist will oversee assay development, validation, and sample analysis, ensuring regulatory compliance and scientific rigor across clinical programs. The position emphasizes collaboration with cross-functional teams, integration of emerging technologies including AI-enabled tools, and contribution to regulatory submissions and data interpretation in a GcLP-compliant environment.
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.
This role involves hands-on execution of immunoassay development, qualification, and clinical sample testing to support Moderna's clinical trials. The technician will prepare reagents, conduct analyses, ensure data quality, and maintain compliance with regulatory standards in a laboratory setting. The position requires full-time on-site work with occasional overtime and is embedded in a collaborative, regulated environment focused on high-quality bioanalytical output.
This role involves leading scientific strategy and execution for immunogenicity and ligand binding assays (LBA) in support of Moderna’s mRNA-LNP therapeutic programs. The Principal Scientist will oversee regulated bioanalytical activities including assay development, validation, and sample analysis, ensuring compliance with GcLP, GLP, and GCP standards. The position plays a key role in clinical development by generating high-quality data to inform regulatory submissions and advance innovative medicines, with opportunities to engage in AI-enabled and digital analytical approaches.
