Latest UK roles, updated daily.
This role involves leading the clinical development of oncology treatments, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading cross-functional teams, and engaging with health authorities and external partners. The position emphasizes leveraging advanced analytics and AI to drive decision-making and innovation in clinical development.
This role involves leading the clinical development of oncology drugs, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading governance discussions, and representing the company in health authority interactions. The role emphasizes data-driven decision-making and leveraging advanced analytics to enhance clinical development.
This role involves performing routine cGMP Quality Control testing, including analytical chemistry and stability testing, to ensure the quality and integrity of materials and products. You will work with advanced analytical technologies and laboratory information systems to support manufacturing, product release, and regulatory compliance.
The Principal Engineer, Drug Product will lead the development of global engineering standards for drug product processes, including filling, inspection, packaging, and labeling. They will manage capital projects, ensure regulatory compliance, and drive innovation in manufacturing technologies across Moderna’s global network.
Design and develop generative protein models that capture enzyme dynamics and function, with a focus on catalysis through motion. Analyze complex datasets and collaborate with interdisciplinary teams to evolve designs in vivo. Contribute to high-impact research publication and translation within a cutting-edge synthetic biology environment.
This role involves advancing interdisciplinary research in materials and devices for life sciences, focusing on nanopore technologies, 3D tissue engineering, and device development for clinical diagnostics and therapeutics. The scientist will design experiments, refine emerging technologies, and contribute to high-impact publications in a collaborative, well-resourced environment. Work spans molecular sciences, nanotechnology, and bioengineering to create transformative biomedical tools.
This role involves leading clinical development for sarcoma within GSK's oncology portfolio, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety monitoring, contribute to regulatory interactions, and represent the programme externally at scientific forums. Based on-site in Waltham, MA, the position requires integration with cross-functional teams and mentorship of clinical staff to ensure patient-centred, scientifically rigorous drug development.
This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials within GSK’s global development programme. The Medical Director provides physician-level expertise in study design, data interpretation, and regulatory engagement, ensuring patient safety and clinical integrity across phases I–III. Working within a cross-functional matrix team, the role integrates medical insight into clinical strategy and collaborates with external experts and investigators to advance innovative cancer therapies.
This role involves leading clinical development in oncology with a focus on sarcoma, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety evaluation, contribute to regulatory interactions, and mentor clinical teams within a matrixed global environment. The position requires deep expertise in oncology drug development and active engagement with external scientific leaders and regulatory authorities.
This role involves leading medical oversight in gastrointestinal (GI) oncology clinical development, ensuring patient safety and clinical integrity across study design, execution, and data interpretation. The Medical Director collaborates with cross-functional teams to integrate physician insights into clinical trials, engages with external experts and regulators, and contributes to regulatory submissions and scientific communications. The position requires deep expertise in oncology and clinical development within a global pharmaceutical environment.
This role involves leading clinical development strategy for sarcoma within GSK's oncology portfolio, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety evaluation, mentor clinical teams, and represent the programme in regulatory and scientific forums. Based on-site at a GSK location with future relocation to Cambridge, UK.
Leads global respiratory epidemiology and real-world evidence initiatives to shape vaccine development, designing and delivering studies on disease burden, treatment patterns, and safety. Works cross-functionally with clinical, regulatory, and external partners, driving scientific strategy and innovation. Involves mentoring staff, managing collaborations, and disseminating findings through publications and regulatory submissions.
Lead global respiratory epidemiology and real-world evidence initiatives to inform vaccine development, designing and delivering studies on disease burden, treatment patterns, and safety. Partner with cross-functional teams and external collaborators to generate regulatory-grade evidence and shape development strategies. Drive scientific dissemination through publications, regulatory submissions, and international conferences.
Leads global respiratory epidemiology and real-world evidence initiatives to inform vaccine development, designing and delivering studies on disease burden, treatment patterns, and safety. Works cross-functionally with clinical, regulatory, and safety teams, manages external collaborations, and drives scientific dissemination through publications and regulatory submissions. Focuses on strategic epidemiological planning and mentoring junior staff within a matrixed R&D environment.
Leads global respiratory epidemiology and real-world evidence initiatives to inform vaccine development, designing studies on disease burden, treatment patterns, and safety. Works cross-functionally with clinical, regulatory, and safety teams, manages external collaborations, and drives scientific dissemination through publications and regulatory submissions. Focuses on strategic epidemiological planning and mentoring junior staff in a matrixed environment.
