Latest UK roles, updated daily.
Leads global safety strategy for formulation safety across the product lifecycle, focusing on clinical safety evaluation, signal detection, and risk management. Oversees production of key pharmacovigilance documents and ensures compliance with regulatory standards. Acts as safety representative in cross-functional teams and drives safety specifications and risk mitigation plans.
Leads global safety strategy for formulation safety within CSL's GSPV department, overseeing clinical safety evaluation across product lifecycles. Responsible for signal detection, risk management planning, and regulatory compliance across clinical development and post-marketing phases. Serves as safety representative in cross-functional teams, ensuring alignment with medical, regulatory, and business objectives.
This role involves hands-on laboratory work and data analysis in genomics, transcriptomics, and single-cell sequencing to support oncology drug discovery. The scientist will develop and optimise NGS workflows, process and interpret complex omics datasets, and collaborate across disciplines to translate findings into scientific insights. Emphasis is placed on integrating experimental and computational approaches, with opportunities to apply AI-enabled tools for enhanced data interpretation and workflow efficiency.
Leads toxicology strategy for immune oncology drug development, integrating regulatory and preclinical safety science to guide candidate selection and regulatory submissions. Works across discovery and development to assess immune-related safety risks of novel immunotherapies. Provides scientific leadership, mentors junior toxicologists, and contributes to licensing decisions and external collaborations.
This role involves hands-on laboratory work supporting immunoassay development and clinical testing for Moderna’s mRNA-based therapeutic programs. The technician will prepare reagents, conduct sample analysis, ensure regulatory compliance, and contribute to high-quality data generation for clinical trials. Based in Oxford, the position requires full-time on-site work in a regulated lab environment with occasional overtime.
This role involves leading the analysis and integration of complex multi-omic datasets—including single-cell and spatial transcriptomics, proteomics, and metabolomics—to generate actionable biological insights that inform drug development decisions. The scientist will work across hepatology, renal, metabolic, and cardiovascular disease areas, applying advanced computational and statistical methods to support target identification, biomarker discovery, and patient stratification. Collaboration with cross-functional teams and external partners is central, with an emphasis on reproducible, scalable code and scientific innovation.
Operate within a GMP-regulated warehouse environment at Moderna’s Harwell site, managing inbound and outbound material flows, inventory control via SAP, and supporting continuous mRNA manufacturing operations. Perform cycle counts, documentation, and logistics coordination while adhering to strict quality and safety standards. Gain exposure to digital-first and AI-enabled tools within a fast-paced, collaborative pharmaceutical setting.
Manages end-to-end contract processes for Investigator Initiated Studies and Supported Collaborative Studies with academic and research institutions. Responsibilities include drafting, negotiating, and finalizing agreements, resolving contractual issues, ensuring timely execution, and supporting clinical development activities within a global biopharma environment.
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.
This role involves building and managing cloud infrastructure and DevOps tooling to support AI-driven drug discovery. You'll work across research, development, and production environments using GCP, Kubernetes, and Infrastructure as Code, collaborating closely with scientists, ML researchers, and engineers. The focus is on creating scalable, secure, and automated systems that accelerate scientific innovation in a fast-moving, interdisciplinary environment.
This role involves developing metabolic engineering and synthetic biology strategies to optimise plant respiratory activity, energy status, and redox balance. Work is conducted in plant cell cultures and whole plants using iterative design–build–test–learn cycles, with translation from lab to real-world applications supported by multi-omics phenotyping and cross-disciplinary collaboration. The scientist will drive IP generation and contribute to commercialising innovations in sustainable agriculture and plant-based production.
Develop and scale experimental platforms to evaluate engineered protein variants' impact on photosynthetic efficiency, photoprotection, and carbon assimilation in plants. Utilize transient expression systems, molecular biology, and advanced phenotyping to accelerate crop productivity research. Collaborate with computational scientists and protein engineers to inform downstream crop transformation decisions.
Develops and optimizes metagenomic extraction and sequencing workflows for diverse sample types, focusing on low-biomass and inhibitor-rich matrices. Works end-to-end from DNA/RNA extraction to library prep, with emphasis on high molecular weight recovery and virology applications. Collaborates globally to enhance data quality and scalability for AI-driven biological discovery.
This role involves leading the development of next-generation drug delivery devices by managing multidisciplinary R&D teams and driving new business opportunities. The consultant will take ownership of programme management while remaining technically engaged in project delivery, supporting innovation in medical technology. A key aspect includes mentoring junior team members and contributing to high-impact, industry-disrupting solutions.
This role involves leading the entire Quality function (QA and QC) within a pharmaceutical manufacturing site, overseeing a team of 15 and ensuring strict adherence to GMP and regulatory standards. The individual will drive the site's Quality strategy, manage audits and inspections (including MHRA and customer audits), and lead continuous improvement initiatives across quality systems, validation, and compliance. With a strong emphasis on leadership and team development, the role sits at the heart of the site’s leadership team and requires strategic oversight alongside hands-on operational involvement.
