Lead clinical development for vascular programmes across early and late-phase studies, shaping clinical plans and study designs to accelerate safe, meaningful medicines for vascular disease. Work cross-functionally with translational science, regulatory, safety, and commercial teams to deliver clinical development strategies and drive innovation in cardiovascular medicine.
Lead clinical development for aging-related programs within GSK’s Respiratory, Immunology & Inflammation Research Unit. Provide clinical and scientific leadership across translational and clinical studies, design development plans, and guide regulatory strategy. Work cross-functionally to advance innovative medicines targeting underlying organ dysfunction and unmet medical needs in aging.
This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with accountability for designing, executing, and interpreting global clinical studies to support regulatory submissions. The individual will act as a key clinical leader, collaborating with cross-functional teams and external stakeholders to shape clinical development plans, trial design, and lifecycle strategies. Expertise in obesity, endocrinology, or chronic weight management is required, along with leadership in managing large-scale clinical programs and regulatory deliverables.
This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, serving as the primary clinical accountable leader for global drug development programs. The position involves end-to-end responsibility for clinical strategy, trial design, regulatory submissions, and cross-functional team leadership across a complex matrix environment. It also includes engagement with external stakeholders, patient advocacy groups, and oversight of safety and lifecycle planning, with a focus on obesity and related therapeutic areas.
Perform on-site installation, maintenance, and repair of advanced medical diagnostic systems in NHS and private laboratories. Provide technical troubleshooting and customer support across complex clinical environments. Receive full product training and work within a globally recognised healthcare technology organisation.
This role involves servicing and repairing advanced medical diagnostic systems in NHS and private laboratory settings, including on-site troubleshooting and breakdown response. The engineer will work with high-value, complex equipment and provide technical solutions directly to laboratory staff. Full product training is provided, and the role requires a flexible schedule with some weekend work.
Leads global medical strategy for a novel CAR-T therapy in autoimmune diseases, driving evidence generation and scientific engagement with key opinion leaders, patient groups, and research institutions. Oversees real-world evidence, registries, and investigator-initiated studies while ensuring compliance and medical governance. Collaborates cross-functionally to shape clinical development, regulatory, and launch strategies in a rapidly evolving immunology landscape.
This role involves leading the end-to-end safety strategy for priority pharmaceutical programs in the Cardio Renal Metabolism (CRM) therapeutic area, from development through lifecycle management. The individual will serve as the scientific safety leader, driving safety governance, benefit-risk assessments, and regulatory interactions, while mentoring teams and embedding safety insights across global functions. It requires deep expertise in pharmacovigilance, cross-functional leadership, and clear communication of complex safety data.
This role involves leading the development, qualification, and execution of complex cell-based immunoassays to support Moderna’s clinical trials across multiple therapeutic areas. The scientist will generate high-quality, reproducible data in compliance with GCP and GLP standards, while serving as a subject matter expert and collaborating with cross-functional teams. Emphasis is placed on innovation, scientific rigor, and advancing mRNA-based medicine through robust assay design and data analysis.
This role involves hands-on execution of immunoassay development, qualification, and clinical sample testing to support Moderna's clinical trials. The technician will prepare reagents, conduct analyses, ensure data quality, and maintain compliance with regulatory standards in a laboratory setting. The position requires full-time on-site work with occasional overtime and is embedded in a collaborative, regulated environment focused on high-quality bioanalytical output.
Manages end-to-end clinical trial operations for 2–3 gene therapy studies, ensuring compliance with global regulatory standards and internal SOPs. Coordinates cross-functional teams, CROs, and vendors to deliver on timelines and budget, with responsibilities spanning protocol development, site selection, data integrity, and risk management. Focuses on patient safety, trial documentation, and operational planning within a rare disease gene therapy context.
Lead clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs, designing studies and guiding regulatory submissions. Oversee modeling and simulation to inform dose selection and accelerate drug development. Collaborate across translational, clinical, and preclinical teams in a tech-driven biopharma environment.
Leads the end-to-end delivery of global clinical trials from start-up to close-out, ensuring compliance, data integrity, and on-time execution. Oversees clinical operations and data management functions, including vendor and site management, database design, and regulatory coordination. Focuses on strategic planning, cross-functional collaboration, and team development within a regulatory-compliant environment.
This role involves supporting the installation, validation, and verification of new laboratory analysers within an NHS clinical chemistry setting. The Biomedical Scientist will ensure equipment meets performance standards, troubleshoot technical issues, and maintain compliance with quality and regulatory requirements. It offers hands-on involvement in a major laboratory transformation project within a modern NHS environment.
This role involves leading regulatory toxicology strategies for late-stage clinical and marketed products across multiple therapy areas, with a focus on safety risk assessment and global marketing applications. The Senior Project Toxicologist provides non-clinical safety expertise, supports regulatory submissions, and mentors teams through the drug development lifecycle. Based in Cambridge, the position operates within a collaborative R&D environment, requiring deep scientific and regulatory knowledge in toxicology.
