This role involves collaborating with scientists and engineers to build robust, reproducible data pipelines for diverse research projects. You will ensure datasets are accurate, version-controlled, and ready for machine learning, working hands-on with cutting-edge technologies and methodologies.
The Senior Group Leader, Industry will lead a transformative research programme in plant biotechnology, focusing on advancing fundamental and applied science in photosynthesis, carbon assimilation, and nitrogen fixation. They will build and manage a high-performing interdisciplinary team, develop cross-sector collaborations, and ensure research excellence is translated into commercial opportunities.
This role involves developing and executing comprehensive (pre)-formulation strategies for small molecules, collaborating with multi-disciplinary teams, and authoring technical reports and regulatory submissions. The position offers opportunities for personal growth and innovation in a cutting-edge AI-driven drug discovery environment.
Develop and optimise cutting-edge AI models at the intersection of machine learning and drug discovery, translating research into scalable, production-ready systems. Work on foundational models like Diffusion networks, Transformers, and GNNs, building robust infrastructure and data pipelines while collaborating closely with scientists. Focus on advancing a digital biology platform to accelerate rational drug design across multiple therapeutic areas.
This role involves leading clinical development for oncology assets, specifically in genitourinary (GU) cancers, within a global matrix environment. The Senior Medical Director will design and execute phase 1–3 clinical trials, provide medical oversight, interpret study data, and engage with external experts and regulatory authorities. The position plays a key strategic role in advancing GSK’s oncology pipeline from development through regulatory approval and lifecycle management.
This role involves developing and executing global and regional regulatory strategies for oncology products across their lifecycle, ensuring compliance and optimal labeling. The manager will collaborate with cross-functional teams and regulatory authorities to support submissions and approvals, leveraging regulatory intelligence to inform decision-making. The position emphasizes strategic planning, stakeholder engagement, and innovation within a patient-focused biopharma environment.
This role involves hands-on laboratory work in cell biology, including designing and executing cellular and biochemical assays, maintaining cell lines, and analyzing data. The position is at the intersection of biology and technology, contributing to the discovery of novel drug targets and working in a fast-paced, interdisciplinary team.
This role involves leading and shaping the cardiac electrophysiology and translational ion channel strategy, guiding multiple drug discovery programmes, and maintaining a presence in the laboratory. Responsibilities include scientific leadership, project management, and mentoring scientists.
The Clinical Research Nurse II conducts multiple ongoing clinical trials, ensuring patient safety and compliance with FDA/GCP and ICH regulations. Responsibilities include scheduling visits, performing study activities, recording data, and maintaining patient relationships.
This role involves leading a project to investigate the function and regulation of SLFN11 in replication stress tolerance, cancer development, and therapy resistance. The postdoctoral fellow will conduct genome-wide CRISPR screens, high-content imaging, and biochemical assays to identify and validate factors that regulate SLFN11 activation.
This role involves designing and implementing generative models to understand cellular behavior from complex biological data. You will collaborate with experimental teams to validate computational hypotheses and guide real-world interventions, pushing the boundaries of generative modeling in a highly interdisciplinary environment.
The Regulatory Affairs Consultant will focus on post-approval CMC activities for biological and plasma products, including developing submission strategies, assessing change controls, and coordinating with various departments to ensure regulatory compliance. The role involves managing projects in Regulatory Information Management systems and mitigating risks associated with regulatory procedures.
This role involves developing and maintaining labeling strategies for pharmaceutical products, including the creation and management of core data sheets, US Prescribing Information, and EU Summary of Product Characteristics. The Senior Consultant will collaborate with various stakeholders to ensure global alignment and compliance, and contribute to clinical study designs and regulatory strategies.
This role involves developing and optimizing advanced formulations for therapeutic delivery, conducting experiments to assess formulation performance, and collaborating with multidisciplinary teams to advance technologies from early-stage development to practical application.
This 12-month industrial placement offers hands-on laboratory experience in structural biology and biophysics, focusing on membrane proteins. You will work closely with scientists to develop practical skills in protein handling, biochemical and biophysical workflows, and electrophysiology-based methods, contributing to early drug discovery efforts.
