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...
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...
Lead the methodological direction of AI-driven workflows, designing model selection frameworks, cohort segmentation, and agent decision logic using real-world healthcare data. Partner with engineering and governance teams to translate analytical rigor into production systems, while mentoring junior scientists and advancing AI innovation across medical and commercial use cases in a regulated pharma environment.
Lead the methodological direction for AI-driven workflows in healthcare, focusing on model selection, cohort design, and agent decision logic using real-world data such as EHR and claims. Collaborate with engineering and governance teams to translate analytical frameworks into production systems, while mentoring junior scientists and advancing AI/ML innovation in a regulated pharmaceutical environment.
This role involves leading toxicology strategy in drug discovery with an AI-first approach, designing safety assessment frameworks, and guiding the development of predictive AI models for toxicity. The candidate will work across small molecules and biologics, collaborate with machine learning teams, oversee outsourced wet-lab studies via CROs, and mentor junior scientists. A key focus is reducing reliance on animal testing through innovative, data-driven toxicology solutions.
Develop and optimise cutting-edge AI models at the intersection of machine learning and drug discovery, translating research into scalable, production-ready systems. Work on foundational models like Diffusion networks, Transformers, and GNNs, building robust infrastructure and data pipelines while collaborating closely with scientists. Focus on advancing a digital biology platform to accelerate rational drug design across multiple therapeutic areas.
Drive target discovery and validation in precision oncology by integrating multimodal biological data (phenomics, transcriptomics, genomics, proteomics) to identify novel therapeutic targets. Collaborate with cross-functional teams to develop scalable computational methods and build compelling data packages that advance drug programs. Develop criteria for target nomination and support early translational strategies using AI-powered platforms.
Lead a team of computational biologists to identify and validate novel oncology targets using integrated phenomics, transcriptomics, genomics, and proteomics data. Develop and scale methods for target discovery in oncology and immunological diseases, collaborating closely with biologists, data scientists, and engineers. Drive data strategy and present findings to stakeholders to advance drug discovery programs.
This senior leadership role involves providing scientific, operational, and strategic leadership for the ADA Immunoassay Bioanalysis function. Responsibilities include managing a high-performing team, ensuring regulatory compliance, overseeing project delivery, and driving business growth through commercial and client relationships.
Operate and maintain equipment in a cGMP-compliant, highly automated mRNA vaccine production environment at Moderna's Oxford facility. Perform production operations, support quality assurance, troubleshoot issues, and contribute to continuous improvement initiatives using digital systems and advanced manufacturing technologies. Work within a 2-2-3 rotating shift pattern to ensure reliable, safe, and compliant vaccine manufacturing.
This role involves operating and maintaining equipment in a cGMP-regulated mRNA vaccine production environment, ensuring safe and compliant manufacturing processes. The associate will execute production operations, support quality assurance, troubleshoot technical issues, and contribute to continuous improvement initiatives. Work is conducted in a highly automated, digitally enabled facility with a focus on operational excellence and innovation in mRNA technology.
This role involves designing and delivering global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, within drug development programs. The individual will lead regulatory submissions across the lifecycle, engage with health authorities, and ensure compliance with global regulations. Collaboration with cross-functional teams and external partners is central to advancing regulatory plans for innovative diagnostics in a hybrid working environment.
This role involves developing and operationalizing international access strategies for immunology assets, shaping payer value propositions, and collaborating with cross-functional teams to maximize patient access to innovative therapies. The Director will also manage resources, anticipate policy trends, and represent Novartis in internal and external stakeholder engagements.
Provide on-site service and repair for advanced medical diagnostic systems used in NHS and private laboratories. Troubleshoot complex technical issues and deliver customer support across clinical environments. Receive full product training and work within a globally recognised healthcare technology organisation.
Provide on-site service and repair for advanced medical diagnostic systems in NHS and private laboratories. Troubleshoot complex technical issues and deliver customer-focused solutions during frequent site visits. Receive full product training and work with cutting-edge diagnostic equipment in a supportive, innovative environment.
