The Associate Director, Global Program Management (Oncology) at GSK will lead the development and execution of integrated project plans for R&D pipeline projects. Key responsibilities include facilitating asset strategy, managing project risks, and ensuring high-quality data and reporting. The role involves working closely with cross-functional teams to optimize project delivery and drive strategic decisions.
The Associate Director, Global Program Management (Oncology) at GSK will lead the development and execution of integrated project plans for R&D pipeline projects. Key responsibilities include facilitating asset strategy, managing project risks, and ensuring high-quality data and reporting. The role involves working closely with cross-functional teams to optimize project delivery and drive strategic decisions.
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.
This role involves leading the creation and management of investigator site budgets and contracts for global clinical trials, using Grants Manager and FMV benchmarking tools. The Senior Manager collaborates with CROs, Legal, and Clinical Operations to ensure site budgets align with study forecasts and are executed on time. Responsibilities include strategic planning, contract negotiation oversight, risk identification, and process improvement within an outsourced trial model.
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.
This role involves developing and optimising high-throughput enzyme assays to characterise plant protein variants for improved crop yield and climate resilience. The scientist will work at the intersection of enzymology, protein engineering, and automation, collaborating with AI and robotics teams to build scalable biochemical workflows. The position focuses on translating computational protein designs into experimentally validated candidates for agricultural innovation.
The Central Monitor (CM) oversees and supports clinical trials through centralized monitoring activities, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure Central Monitoring technology, and provide ongoing data surveillance and risk management.
The Central Monitor (CM) is responsible for overseeing clinical trials through centralized monitoring, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure monitoring technology, and communicate findings to stakeholders.
This role involves producing and characterising recombinant proteins for molecular glue discovery, using mammalian cell expression systems. The technician will support biochemical and biophysical assays, maintain lab equipment, and train new users in a multidisciplinary research environment.
This role involves managing clinical trials, including providing support on approval processes, trial management, recruitment strategies, and data quality. The position is part of the Tayside Clinical Trials Unit (TCTU) and focuses on both new and established drug and complex intervention trials, with a lead role in the BE-Genomics trial.
This role involves designing and prototyping generative machine learning models for protein design, with a focus on real-world biological functionality. The scientist will build scalable data pipelines, optimize model performance, and collaborate closely with biologists to test predictions in wet lab environments. A strong research background and passion for interdisciplinary innovation are essential.
Build and maintain scalable AI systems that integrate large language models with biomedical research tools, focusing on agent development, data workflows, and deployment within a multidisciplinary environment. Work on real-time, interactive systems that empower researchers through robust backend engineering and AI integration.
This role involves leading the Genomics Hub operations, managing genomics resources, and providing technical guidance to scientific teams. Responsibilities include workflow management, data management, project oversight, and technology development. The position requires deep expertise in NGS workflows and strong leadership skills.
Design and develop novel generative machine learning models for protein design, integrating with wet lab experiments to validate performance in real-world biological contexts. Collaborate closely with interdisciplinary teams of researchers, engineers, and biologists while maintaining robust, scalable code and infrastructure. Focus on rapid prototyping, model optimization, and continuous learning from experimental feedback to advance synthetic biology.
The Head of External Drug Discovery Operations will lead the strategic and operational aspects of externalised drug discovery and preclinical research, partnering with internal teams and CROs to ensure high-quality, high-throughput data generation and integration into AI-driven workflows. The role involves managing a team, establishing vendor relationships, and driving innovation in external research operations.
