This role involves providing medical leadership within GSK's oncology clinical development team, focusing on genitourinary (GU) cancers. The Medical Director will lead medical monitoring, ensure patient safety, interpret clinical data, and contribute to study design and regulatory submissions. Working closely with cross-functional teams, the role integrates physician-level insight into clinical strategy and drug development execution.
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 role emphasizes data-driven decision-making and leveraging advanced analytics to enhance clinical development.
This role involves leading the reliability and scalability of AI/ML infrastructure for biotech applications, focusing on GPU/TPU systems, workload orchestration, and inference services. The engineer will overhaul monitoring, improve CI/CD stability, and ensure robust platform performance to support cutting-edge drug discovery research. Close collaboration with research and applied ML teams is central to the role.
Lead the development and execution of bioanalytical strategies for a diverse portfolio of AI-designed therapeutics, including small molecules, biologics, and ADCs. Design and validate PK, PD, and immunogenicity assays, manage global CROs, and integrate bioanalytical data into AI models to refine drug discovery. Play a key role in IND-enabling studies and cross-functional preclinical development in a hybrid London-based role.
Leads global regulatory strategy for CMC (Chemistry, Manufacturing, and Controls) in support of mRNA-based medicines, ensuring compliance with international regulations and guiding submissions across multiple therapeutic areas. Works closely with manufacturing, quality, and development teams to prepare high-quality regulatory documentation and engage with health authorities. Focuses on biologics, particularly in vaccines, oncology, and rare diseases, within a rapidly expanding biotech environment.
This role involves developing, qualifying, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RT-qPCR—to support clinical pharmacokinetic and pharmacodynamic studies within a GCLp-compliant environment. The scientist will work closely with cross-functional teams to ensure robust data generation, maintain regulatory compliance, and integrate emerging digital and automation technologies into workflows. A strong focus on reagent management, assay documentation, and continuous process improvement is central to the position.
Lead global respiratory epidemiology and real-world evidence initiatives to inform vaccine development, designing and delivering studies on disease burden, treatment patterns, and safety. Partner with cross-functional teams and external collaborators to generate regulatory-grade evidence and shape development strategies. Drive scientific dissemination through publications, regulatory submissions, and international conferences.
Leads global respiratory epidemiology and real-world evidence initiatives to inform vaccine development, designing and delivering studies on disease burden, treatment patterns, and safety. Works cross-functionally with clinical, regulatory, and safety teams, manages external collaborations, and drives scientific dissemination through publications and regulatory submissions. Focuses on strategic epidemiological planning and mentoring junior staff within a matrixed R&D environment.
Leads global respiratory epidemiology and real-world evidence initiatives to inform vaccine development, designing studies on disease burden, treatment patterns, and safety. Works cross-functionally with clinical, regulatory, and safety teams, manages external collaborations, and drives scientific dissemination through publications and regulatory submissions. Focuses on strategic epidemiological planning and mentoring junior staff in a matrixed environment.
Leads global respiratory epidemiology and real-world evidence initiatives to shape vaccine development, designing and delivering studies on disease burden, treatment patterns, and safety. Works cross-functionally with clinical, regulatory, and external partners, driving scientific strategy and innovation. Involves mentoring staff, managing collaborations, and disseminating findings through publications and regulatory submissions.
This role involves leading CMC regulatory strategy for global mRNA product development, preparing and reviewing regulatory submissions, and guiding cross-functional teams on compliance and agency interactions. The position requires deep expertise in biologics CMC regulations, particularly in EU and ROW markets, and plays a key part in shaping regulatory pathways across vaccines, oncology, and rare diseases. Based at the Harwell site, it emphasizes in-office collaboration within a multidisciplinary team.
This role involves performing routine environmental monitoring, water sampling, and microbiological testing (including sterility, bioburden, and endotoxin) for mRNA products in a GMP-regulated manufacturing environment. The analyst will support method transfers, data review, investigations, and compliance activities while working closely with internal teams and contract laboratories. Emphasis is placed on digital workflows, data integrity, and adherence to cGMP standards.
The VP, Medicine Development Leader for Cancer Vaccines will lead the global development of GSK's cancer vaccine, from early stages through approval and launch. Key responsibilities include strategic vision, team leadership, and collaboration with various stakeholders across R&D and commercial functions to ensure successful development and market entry.
The VP, Medicine Development Leader for Cancer Vaccines will lead the global development of GSK's cancer vaccine, working with cross-functional teams to define the strategic vision and operational plan. Key responsibilities include managing the development team, ensuring regulatory approval, and aligning with GSK's oncology strategy.
The VP, Medicine Development Leader for Cancer Vaccines will lead the global development of GSK's cancer vaccine, working with cross-functional teams to define the strategic vision and operational plan. Key responsibilities include managing the development team, ensuring regulatory approval, and aligning with GSK's oncology strategy.
