Latest UK roles, updated daily.
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.
The Medical Director, Oncology Clinical Development role involves leading medical monitoring, safety oversight, and clinical data interpretation for clinical studies in lung and head/neck cancers. The role requires strong clinical expertise, collaboration with cross-functional teams, and engagement with external experts to ensure patient safety and study integrity.
The Principal Engineer, Drug Product will lead the development of global engineering standards for sterile drug product processes, including filling, inspection, packaging, and labeling. They will manage capital projects, ensure regulatory compliance, and drive innovation in manufacturing technologies across Moderna’s global network.
This role involves operating and maintaining equipment in a cGMP-regulated mRNA vaccine production environment, ensuring safe and compliant manufacturing processes. The associate will execute production operations, support quality assurance, troubleshoot technical issues, and contribute to continuous improvement initiatives. Work is conducted in a highly automated, digitally enabled facility with a focus on operational excellence and innovation in mRNA technology.
Conduct independent, high-impact research in a multidisciplinary environment focused on engineering biology, with responsibilities including experimental design, data analysis, publication, and mentoring junior researchers. Work at the intersection of biology, technology, and engineering within a newly established, well-resourced institute pursuing transformative solutions in health, agriculture, and sustainability.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, protocol development, and collaboration with cross-functional teams and external experts.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. This role involves leading medical monitoring, ensuring patient safety, and collaborating with cross-functional teams to integrate medical considerations into study execution and regulatory interactions.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, and collaboration with cross-functional teams to ensure patient safety and clinical integrity.
The Medical Director, Oncology Clinical Development is responsible for providing medical expertise in the design, conduct, and interpretation of clinical studies for lung and head/neck cancers. Key responsibilities include medical monitoring, safety oversight, and collaboration with cross-functional teams to ensure patient safety and clinical integrity.
This role involves leading the clinical development strategy for GSK's Hematology portfolio, from early-phase studies to market launch. Responsibilities include shaping scientific approaches, managing cross-functional teams, and ensuring regulatory compliance. The role emphasizes innovation, collaboration, and patient-centric focus.
This role involves leading the clinical development strategy for GSK's hematology portfolio, from early-phase studies to market launch. Responsibilities include shaping scientific approaches, managing cross-functional teams, and ensuring regulatory compliance. The role emphasizes innovation, patient-centric focus, and strong leadership.
This role involves leading the clinical development strategy for GSK's hematology portfolio, from early-phase studies to market launch. Responsibilities include shaping scientific approaches, managing cross-functional teams, and ensuring regulatory compliance. The role requires deep expertise in hematology/oncology and a proven track record in clinical trial design and execution.
This role involves leading the clinical development strategy for GSK's Hematology portfolio, from early-phase studies to market launch. Responsibilities include shaping scientific approaches, managing cross-functional teams, and ensuring regulatory compliance. The role requires extensive experience in oncology clinical development and leadership.
This role involves leading clinical development in oncology with a focus on sarcoma, providing medical oversight and strategic input across study design, execution, and data interpretation. The position ensures patient safety and clinical integrity while guiding cross-functional teams and engaging with external experts. It requires deep expertise in oncology drug development and strong leadership in a matrixed global environment.
This role involves serving as the physician lead within an oncology clinical development team, providing medical expertise in study design, safety oversight, and data interpretation for gastrointestinal (GI) cancer trials. The Medical Director ensures patient safety and clinical integrity across clinical studies, collaborates with cross-functional teams and external experts, and contributes to regulatory submissions and scientific communications. The position supports GSK’s mission to advance innovative cancer treatments grounded in disease biology and real-world impact.
