Latest UK roles, updated daily.
This role involves driving the AI-native Development Operations strategy at GSK, identifying and prototyping AI opportunities, and leading the deployment of AI-enabled workflows. The Director will work with business SMEs, technology teams, and external partners to ensure scalable and compliant solutions.
This role involves leading the clinical development of oncology treatments, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading governance discussions, and representing the asset in external engagements. The role emphasizes data-driven decision-making and leveraging advanced analytics.
This role involves developing and refining bioinformatics workflows to analyse whole genome and metagenomic sequencing data for infectious disease diagnostics. The bioinformatician will work closely with wet lab scientists to interpret complex datasets, focusing on taxonomic classification, antimicrobial resistance prediction, and strain characterisation. The position supports a translational research initiative aiming to deploy scalable diagnostic tools globally.
This role involves leading the creation and management of investigator site budgets and contracts for clinical trials, using Grants Manager and FMV benchmarking tools. The candidate will oversee CRO activities, ensure budget consistency across trials, and support timely site activation by managing negotiations and identifying risks. Collaboration with legal, clinical operations, and external partners is central to ensuring compliance and efficiency in contract execution.
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.
Design and develop microfluidic systems for a point-of-care diagnostic device that enables metagenomic sequencing through a cartridge-based interface. Work closely with cross-functional teams to integrate microfluidics with instrumentation, electronics, and firmware, focusing on robustness, automation compatibility, and real-world performance. Conduct prototyping, testing, and validation using techniques like soft lithography and rapid prototyping to advance decentralized infectious disease diagnostics.
This role involves leading clinical development for oncology, specifically in lung cancer, by providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety monitoring, contribute to regulatory interactions, and mentor junior medical staff. The position requires deep expertise in oncology clinical trials and close collaboration with cross-functional teams and external experts.
This role involves leading oncology clinical development for lung cancer programmes, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director ensures patient safety, contributes to regulatory engagements, and mentors medical teams within a cross-functional environment. The position integrates physician expertise into clinical strategy and external scientific forums, focusing on advancing care in high unmet need cancers.
This role involves leading clinical development in oncology, with a focus on lung cancer, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety monitoring, contribute to regulatory interactions, and mentor junior medical staff within a global matrix team. The position emphasizes strategic input, external scientific engagement, and integration of clinical insights to advance therapies for high unmet need.
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 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 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 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 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.
