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This role involves leading the development and delivery of strategic life sciences partnerships for the South West Secure Data Environment (SWSDE). Responsibilities include building relationships with life science organizations, developing commercial models, and ensuring governance and ethical standards are maintained.
The Head of Operational Excellence leads process improvement activities and staff, aligning projects with business strategies. They establish and maintain performance metrics, manage operational processes, and oversee training and development of subject matter experts in a regulated, global matrix organization.
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 leads the identification, evaluation, and advancement of early-stage external innovation opportunities in the Cardiovascular/Renal therapeutic area. The individual will shape sourcing strategies, co-lead cross-functional assessment of new product opportunities, and drive due diligence and transaction execution in collaboration with Business Development. Embedded in the Therapeutic Area Leadership Team, the position plays a strategic role in portfolio development and external engagement with biotech, academia, and investors.
Leads strategic sourcing and evaluation of early-stage (preclinical to Phase 1) external innovation opportunities in the Cardiovascular/Renal therapeutic area. Drives due diligence, shapes partnering strategies, and collaborates with Business Development to execute transactions. Embedded in the Therapeutic Area Leadership Team to align external innovation with portfolio planning.
Leads strategic sourcing and evaluation of early-stage innovation in haematology, from preclinical to Phase 1 assets. Drives due diligence, shapes partnering strategies, and executes transactions in collaboration with Business Development. Embedded in the Therapeutic Area Leadership Team to influence portfolio planning and external innovation priorities.
A little outside Reading, but within reach.
The Clinical Development Medical Director is responsible for providing medical and scientific oversight for clinical trials, ensuring patient safety, and contributing to the design and execution of clinical studies. They will also participate in safety reviews, interact with healthcare professionals, and support regulatory activities.
This role involves servicing a wide range of biomedical devices, including high-complexity medical lasers. You will receive ongoing training and certification, cover a London patch with occasional travel, and enjoy a work-life balance through time off in lieu for excess hours.
As a Senior Software Engineer at EIT, you will design and build robust, scalable software systems that power scientific applications and products. Your responsibilities include creating APIs, CLI tools, and software modules, integrating ML inference servers, hardware interfaces, and data pipelines, and ensuring high availability and low latency. You will work closely with a multi-disciplinary team and champion software engineering best practices.
This role involves leading the development of innovative metabolic engineering and synthetic biology approaches to optimize plant respiratory activity, energy status, and redox balance. The scientist will design and implement engineering strategies, conduct experiments in plant cell cultures and whole plants, and collaborate with multidisciplinary teams to translate research into real-world solutions.
Support translational research by assisting in normothermic machine perfusion experiments and a range of laboratory techniques including cell culture, flow cytometry, and molecular biology. Contribute to gene therapy development using advanced in vitro models, with training provided and no prior perfusion experience required.
Lead and maintain the Quality Management System (QMS) in a regulated diagnostic manufacturing environment, ensuring compliance with ISO standards and audit readiness. Drive quality documentation, process improvements, and cross-functional collaboration with technical and operations teams. Play a key role in upholding product safety and quality within a growing, innovative business.
This role involves building and operating a scalable, secure cloud platform to support scientific research and experimentation. The engineer will implement CI/CD and GitOps pipelines, enforce policy-as-code with Kyverno, and develop monitoring and self-service infrastructure for research workloads ranging from Python notebooks to distributed GPU clusters.
Develop and lead a plant cell-based screening platform to evaluate carbon fixation and photosynthetic efficiency, using suspension cultures and genetic engineering techniques like CRISPR. Identify improved enzyme variants and metabolic pathways, then validate top candidates in whole plants to enhance crop performance. Work within a multidisciplinary team to drive discovery from lab to scalable agricultural solutions, with strong emphasis on IP generation and ethical innovation.
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