This role involves leading the clinical development of oncology drugs, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading governance discussions, and representing the company in health authority interactions. The position requires strong scientific and leadership skills, with a focus on leveraging data and technology to drive clinical development.
This role involves leading the clinical development of oncology treatments, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading governance discussions, and representing the asset in external engagements. The role emphasizes data-driven decision-making and leveraging advanced analytics.
Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna's Harwell site, ensuring compliance with GxP and safety standards. Establish maintenance strategies, lead capital projects, and drive continuous improvement using engineering excellence principles. Work closely with global teams and support digital integration in a high-growth biotech environment.
This role involves hands-on mRNA vaccine production operations at Moderna’s Harwell facility, adhering to cGMP standards and collaborating with Quality Assurance. Responsibilities include operating production equipment, maintaining documentation, troubleshooting issues, and contributing to continuous improvement and digital innovation.
This role involves leading communications and strategy initiatives to support R&D priorities in the Office of the Chief Scientific Officer. You will collaborate with senior leaders, develop clear scientific narratives, and ensure effective stakeholder engagement. The position emphasizes translating complex science into accessible and inspiring stories.
The AI Director role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to improve clinical trial outcomes. Responsibilities include leading the prioritization of AI opportunities, building and testing prototypes, and shaping deployment strategies with cross-functional teams.
This role involves leading communications and strategy initiatives to support R&D priorities in the Office of the Chief Scientific Officer. You will collaborate with senior leaders, develop clear scientific narratives, and ensure effective communication to diverse stakeholders.
This role involves driving the AI-native Development Operations strategy at GSK, identifying and prototyping AI opportunities, and leading the deployment of AI-enabled workflows. The Director will work with business SMEs, technology teams, and external partners to ensure scalable and compliant solutions.
This role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to improve clinical trial outcomes. Responsibilities include leading the prioritization of AI opportunities, building and testing prototypes, and shaping deployment strategies with cross-functional teams.
This role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to improve clinical trial outcomes. Responsibilities include leading AI opportunity prioritization, building and testing prototypes, and shaping build-buy-partner decisions.
This role involves driving the AI-native Development Operations strategy at GSK, focusing on identifying and deploying AI solutions to improve clinical trial outcomes. Responsibilities include leading the prioritization of AI opportunities, building and testing prototypes, and shaping deployment strategies with cross-functional teams.
This role involves developing, optimizing, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RNA isolation—to support mRNA-based clinical programs. The scientist will work within GCL0-compliant (GCLP) frameworks to generate pharmacokinetic and pharmacodynamic data, ensuring regulatory compliance and data integrity. Collaboration with cross-functional teams and adoption of digital tools and automation are key to advancing clinical trial execution and analytical processes.
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.
Operate production equipment for mRNA vaccine manufacturing in compliance with cGMP and safety standards. Perform routine maintenance, support deviation investigations, and contribute to continuous improvement in a highly regulated, technology-driven environment. Work collaboratively with QA and cross-functional teams to ensure timely batch disposition and operational excellence.
This role involves performing routine environmental monitoring, water sampling, and microbiological testing to support GMP quality control for mRNA products. The analyst will execute tests including sterility, bioburden, endotoxin, and TOC, while supporting method transfers, validations, and compliance with cGMP standards. The position requires strong documentation practices, collaboration with cross-functional teams, and active participation in quality systems such as investigations and audits.
