This role involves leading the development and application of quantitative systems pharmacology (QSP) models to advance drug discovery and development. Responsibilities include building mechanistic models, collaborating with cross-functional teams, and driving model-informed drug development strategies.
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.
As Lead Central Monitor, you will lead a team of Central Monitors, shaping monitoring strategies to ensure patient safety and data integrity in clinical trials. You will work across clinical, data, and risk-surveillance teams to translate complex risk signals into actionable insights and drive continuous improvement through analytics and technology.
As Lead Central Monitor, you will lead a team of Central Monitors, shape monitoring strategies, and ensure data integrity and patient safety in clinical trials. You will work across clinical, data, and risk-surveillance teams to translate complex risk signals into actionable insights and drive continuous improvement through analytics and technology.
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.
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, regulatory-compliant data using advanced immunological techniques and serve as a subject matter expert within cross-functional teams. Emphasis is placed on innovation, scientific rigor, and integration of emerging technologies including digital and AI-enabled workflows in a GCP/GLP-regulated environment.
This role focuses on end-to-end quality oversight of external vendors and suppliers involved in regulated R&D activities, ensuring compliance with GLP, GCP, GMP, and GVP standards. The individual will lead vendor qualification, audit management, quality agreement negotiation, and continuous performance monitoring, while collaborating with cross-functional teams including Clinical, CMC, Safety, and Legal. A key aspect is driving compliance, data integrity (ALCOA+), and continuous improvement across third-party partners through risk-based assessments, CAPA follow-up, and QMS integration.
This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation into portfolio planning. The position requires deep clinical expertise, a proven track record in deal-making, and strong collaboration with cross-functional teams.
The Cell Therapy Account Executive (CTAE) is responsible for developing and maintaining strong relationships with Advanced Therapy Treatment Centers (ATTCs) in the South UK. Key responsibilities include driving the utilization of Autolus' CAR T therapies, coordinating cross-functional activities, and ensuring a seamless customer experience. The role involves significant travel and requires deep clinical expertise in haematology and oncology.
The Associate Director, Apheresis & Infusion Operations manages the onboarding and ongoing performance of Apheresis and Treatment Centres for Autolus' CAR T-cell therapies. Key responsibilities include fostering relationships with centre staff, resolving technical issues, and ensuring sites are prepared for collections. The role involves up to 50% travel within the UK and occasionally to other regions, primarily within the EU.
The Product Definition Lead will guide the technical direction of complex point-of-care platforms, translating business and clinical needs into clear system requirements. You will lead a multidisciplinary team, manage requirements engineering, and support the development of medical devices and diagnostics.
The Information Security Manager will lead information security, product cybersecurity, and cyber risk management in a growing, highly regulated digital health technology environment. Key responsibilities include maintaining the ISMS, conducting risk assessments, overseeing penetration testing, and embedding cybersecurity in software development processes.
This role involves building relationships with surgical professionals, identifying commercial opportunities, and providing hands-on support during surgical procedures. Responsibilities include product demonstrations, training, and maintaining an accurate sales pipeline through Salesforce.
This senior role involves leading a specialist team to deliver major diagnostic solutions in haematology and coagulation across the UK and Ireland. Responsibilities include managing the tender lifecycle, building relationships with pathology networks, and supporting product lifecycle management. The role also focuses on coaching and developing the ICS team and driving continuous improvement.
This role involves designing and executing biological screening cascades to validate computational predictions in drug discovery. The scientist will lead biophysical, biochemical, and cellular assay development, collaborate with CROs, and bridge AI-driven insights with experimental validation across oncology and immunology programs. Close collaboration with medicinal chemistry, structural biology, and machine learning teams ensures data informs rational drug design.
