This role involves building and maintaining financial and operational models, forecasts, and dashboards to support R&D portfolio and investment decisions. You will work closely with the Head of Data Science and the Finance Portfolio Analytics Manager, collaborating across various teams to turn data into actionable insights.
Lead scientific input into oncology clinical trial design, data interpretation, and regulatory documentation within a global pharmaceutical environment. Contribute to study-level execution and strategic insights while collaborating across multidisciplinary teams. Focus on advancing cancer therapies with high unmet need through rigorous clinical science and cross-functional partnership.
Lead the development and execution of CMC regulatory strategies for mRNA-based products across global submissions, including IND/CTA/BLA/MAA filings. Provide expert guidance on regulatory compliance, interact with health authorities, and support quality and manufacturing teams through change controls and submissions. Work within a multidisciplinary team at the Harwell site to advance Moderna’s pipeline in vaccines, oncology, and rare diseases.
This role involves designing and executing bioanalytical and immunogenicity strategies to support mRNA-based therapeutic development. The scientist will lead assay development for clinical programmes using platforms like ELISA, MSD, and cell-based methods, ensuring regulatory compliance and robust data generation. The position emphasizes collaboration across multidisciplinary teams and integration of digital tools and AI to advance Moderna's pipeline.
This role involves servicing, installing, repairing, and calibrating sophisticated scientific and laboratory X-ray systems used in pharmaceutical and research environments. The position requires a background in field service engineering with experience in high-value capital equipment and a qualification in electronics.
This role involves servicing, installing, repairing, and calibrating sophisticated laboratory X-ray systems in pharmaceutical and research environments. The position requires a background in field service or technical support with experience in high-value capital equipment and electronics.
This role involves aseptically collecting environmental monitoring and cleaning validation samples in sterile manufacturing environments, performing microbiological and QC testing, managing samples through their lifecycle, and ensuring compliance with GMP and client procedures. The role operates on a rotating 2-week shift pattern with 11-hour day shifts.
This role involves testing raw materials, stability samples, in-process samples, and finished products using validated and compendial methods. You will operate and troubleshoot analytical equipment, lead investigations, and mentor junior analysts, ensuring all work meets GMP and data integrity standards.
The Senior Scientist will design, coordinate, and oversee preclinical in vivo studies for oncology pipelines, working closely with CROs and internal teams. Key responsibilities include study design, data analysis, and strategic interpretation to drive candidate optimization and pipeline progression.
The Senior Scientist, Toxicology role involves designing and conducting human-relevant toxicology studies, acting as a Study Director, and leading client-facing activities. Responsibilities include managing scientific projects, training junior scientists, and advancing New Approach Methodologies in toxicology and bioanalysis.
This role involves developing and optimizing LC-MS workflows for single-cell proteomics and metabolomics, supporting researchers in experimental design and data interpretation, and collaborating with multidisciplinary teams to advance cutting-edge mass spectrometry techniques. The position is ideal for a scientist who enjoys method development, troubleshooting, and translating advanced MS technologies into high-impact research.
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 end-to-end clinical trial material planning, vendor management, packaging, labeling, inventory management, and global distribution. You will work closely with Clinical Operations and the Clinical Development team to ensure seamless clinical trial execution and compliance with regulatory standards.
This role involves hands-on administration, configuration, and continuous improvement of an Electronic Lab Notebook (ELN) platform to support R&D and Technical Development laboratories. The scientist will define ELN standards, design workflows and templates, integrate systems, and develop data repositories to enable data-driven decision-making. Collaboration with cross-functional teams is essential to ensure compliance, data integrity, and effective use of the ELN across scientific operations.
The QA Engineer will design, build, and maintain automated test frameworks using Java, Selenium, and RestAssured, ensuring high-quality software delivery. They will work closely with Agile teams to improve test coverage, automate testing, and support continuous integration and delivery processes.
