This role involves leading the clinical development strategy for GSK's hematology portfolio, from early-phase studies to market launch. Responsibilities include shaping scientific approaches, managing cross-functional teams, and ensuring regulatory compliance. The role emphasizes innovation, patient-centric focus, and strong leadership.
The Associate Director (Scientific Data and Publications) manages GSK's external scientific content and data licenses, ensuring cost-effective and compliant access to critical information. The role involves strategic portfolio management, vendor relationships, and leveraging AI for future needs.
This role involves servicing, installing, repairing, and calibrating sophisticated diagnostic systems in pathology departments and NHS laboratories. You will support flow cytometry, cell separation, and diagnostics products, requiring a strong background in electronics or electro-mechanical service and excellent customer service skills.
This role involves servicing, installing, repairing, and calibrating sophisticated medical diagnostic systems in pathology departments and NHS laboratories. You will support flow cytometry, cell separation, and diagnostics products, ensuring they function optimally at customer sites.
This role involves designing and executing experiments in synthetic chromosome engineering, with a focus on centromere design, mitotic segregation, and meiotic control in mammals and plants. The researcher will develop novel methodologies, analyse genomic datasets, and contribute to foundational work in programmable synthesis of large genetic systems. Collaboration, publication, and mentoring are key components, within a multidisciplinary team advancing the engineering of biology.
Develop and scale experimental platforms to evaluate engineered protein variants' impact on photosynthetic efficiency, photoprotection, and carbon assimilation in plants. Utilize transient expression systems, molecular biology, and advanced phenotyping to accelerate crop productivity research. Collaborate with computational scientists and protein engineers to inform downstream crop transformation decisions.
This role involves providing technical leadership for facility and utility systems at Moderna’s biotech manufacturing site in Harwell. The Facilities Engineering Manager ensures operational reliability, oversees vendor performance, and drives maintenance excellence across R&D and manufacturing environments. The position emphasizes continuous improvement, compliance, and the use of digital tools including AI-enabled systems, within a GMP-regulated setting.
This role involves hands-on engineering support for packaging and process automation at Moderna's Harwell facility. Responsibilities include troubleshooting and optimizing PLCs, control systems, and packaging equipment, ensuring compliance and continuous improvement in manufacturing operations.
This role involves working in Pfizer's Regulatory Strategy department, contributing to the development and implementation of regulatory strategies for innovative medicinal products. Responsibilities include compiling regulatory documents, engaging with health authorities, and maintaining systems and processes. The position offers a unique overview of the pharmaceutical product life cycle from research to market.
This role involves designing and developing internal applications and web-based tools to support scientific research and drug discovery. You will work with JavaScript/TypeScript, React, .NET/C#, and Python, and collaborate closely with bioinformaticians, data scientists, and biologists.
This role involves overseeing the quality and compliance of external partners in GLP-regulated nonclinical research, including CROs and laboratories. Responsibilities include vendor qualification, risk-based monitoring, audit coordination, and ensuring adherence to regulatory standards. The role requires deep knowledge of GLP, GCP, and GMP regulations and strong cross-functional collaboration.
The Associate Director, Biostatistics, leads statistical contributions to clinical development programs, including study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing, and ensure the quality and timeliness of deliverables.
This role involves developing an independent, externally funded research programme in AI and One Health Biomedical Data Sciences, collaborating with researchers across disciplines, and contributing to teaching at undergraduate and postgraduate levels. The focus is on addressing major health challenges using AI and data science, with opportunities to work with NHS organisations and industry partners.
This role involves leading early-phase clinical development (Phase 1 and 2) of novel gastroenterology therapies, with a focus on inflammatory bowel disease (IBD). The Translational Medicine Expert will design clinical development plans, serve as medical lead for trials, and collaborate closely with research, biomarker, and late-phase development teams. The position requires strong scientific leadership, engagement with key opinion leaders, and active involvement in regulatory interactions.
This role involves leading early clinical pharmacology studies from protocol development to finalisation, ensuring high-quality data and informed program decisions. The Senior Clinical Pharmacology Trial Leader will work closely with internal teams, investigators, and CROs, overseeing study execution and risk management.
