This role involves leading the generation and dissemination of real-world evidence and health outcomes research for GSK's RSV vaccines. Responsibilities include managing data generation plans, collaborating with cross-functional teams, and engaging with external stakeholders to ensure robust evidence supports product positioning and market access.
This role involves servicing, installing, repairing, and calibrating sophisticated medical laboratory automation systems across Europe. You will support scientific products in various settings, including pathology departments, university research labs, and pharmaceutical environments, with extensive travel and frequent overnight stays.
This role involves servicing, installing, repairing, and calibrating sophisticated medical laboratory automation systems across Europe. You will work with a variety of scientific products in pathology departments, research labs, and pharmaceutical environments, requiring extensive travel and frequent overnight stays.
The Head of Clinical Operations oversees the execution and delivery of clinical studies across multiple therapy areas and development phases in the UK and associated countries. Responsibilities include leading teams, ensuring compliance, and driving operational efficiency and quality.
This role involves conducting advanced research in synthetic evolution, focusing on macromolecular sequence-function relationships and accelerated gene evolution using in vivo systems like OrthoRep. The postdoc will generate large-scale datasets for antibodies and enzymes, explore de novo gene function emergence, and integrate experimental work with machine learning design models. The position emphasizes innovation, collaboration, and translating findings into scalable biological solutions.
This role involves pioneering research in synthetic biology, focusing on genome synthesis and genetic isolation to enable safe, scalable biotechnological applications. The postdoctoral fellow will develop novel methods for genome recoding, engineer synthetic genetic codes, and contribute to foundational work in making biology programmable. Work integrates experimental and computational approaches within a multidisciplinary, mission-driven research environment.
This role involves developing, validating, and executing ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data in a regulated GcLP environment, manage critical reagent characterization, and contribute to clinical sample testing using Watson LIMS. The position emphasizes scientific rigor, regulatory compliance, and collaboration within a high-performance team advancing novel bioanalytical assays.
Develops and validates ligand-binding and cell-based assays to support clinical programs for mRNA medicines. Performs pharmacodynamic and immunogenicity testing in compliance with GcLP, using platforms like Thermo Watson LIMS. Contributes to assay development, reagent management, and regulatory documentation in a fast-paced, innovative lab environment.
The Statistician will provide statistical expertise and support across R&D, clinical, product support, and marketing functions. Key responsibilities include designing and analyzing studies, developing product algorithms, and communicating statistical findings to both technical and non-technical audiences.
This role focuses on building advanced operational models and simulations to optimise Autolus' end-to-end processes across manufacturing, testing, supply chain, and quality. The individual will integrate data from multiple systems to create analytical frameworks that drive strategic decisions, improve capacity planning, and support business cases. It is a highly technical, insight-driven position requiring deep expertise in data modelling, cross-functional collaboration, and problem-solving in a regulated biopharmaceutical environment.
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 leading the Clinical Method Development and Validation team, overseeing bioanalytical method delivery, and ensuring compliance with GLP standards. Responsibilities include optimizing analytical systems, managing a team, and driving continuous improvement in a cutting-edge research environment.
This role leads the statistical strategy for clinical development programs, overseeing study design, data analysis, and regulatory submissions. The individual will guide biostatistical input across trials, interact with regulatory authorities, and ensure accurate reporting of results. Collaboration with cross-functional teams and oversight of internal or outsourced programming efforts are key aspects of the position.
The Central Monitor (CM) oversees and supports clinical trials through centralized monitoring activities, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure Central Monitoring technology, and provide ongoing data surveillance and risk management.
The Central Monitor (CM) oversees and supports clinical trials through centralized monitoring activities, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure Central Monitoring technology, and provide ongoing data surveillance and risk management.
