Biotechnology Jobs

• London
• US$268,000 – US$384,000 pa
• Lead

Conducts original computational biology research for AI safety, investigating how LLMs, specialised biological models, agents and automated laboratories combine to change what is biologically feasible. Spans protein and nucleic-acid design, cellular systems and biological delivery, translating risk judgments into dual-use policy boundaries, evaluation priorities and mitigation requirements alongside threat modellers and red-teamers.

LLMs · Agents · Automated Laboratories +1

• Saffron Walden
• Hybrid
• £38,570 – £49,893 pa
• Senior
• Contract

Develop and apply statistical and deep learning methods to cell-free DNA from pregnant women, calling fetal and maternal genotypes from high-coverage sequence data and building methylation-aware biomarkers for pregnancy complications. Work spans methods development, large cohort application and collaboration with international partners in a statistical genomics group.

Python · R · Unix +6

• Saffron Walden
• Hybrid
• £38,570 – £49,893 pa
• Entry level
• Contract

A postdoctoral research role analysing large-scale human genetic, epigenetic and proteomic datasets, including dried blood spots, birth cohorts and cell-free DNA, to uncover the genetic basis of early-life traits and develop biomarkers for pregnancy and neonatal conditions. The work spans statistical genetics, multi-omics and methods development, with scope to tailor projects to the fellow's interests.

GitHub · Snakemake · Nextflow +1

• London
• £60,000 – £75,000 pa
• Senior · manages people

Lead the UK scientific affairs strategy for an international probiotic and functional food organisation, acting as senior scientific authority. Build KOL relationships across academia and healthcare, oversee human studies and research, ensure claims meet regulations, and manage a scientific affairs team while collaborating with European and global colleagues.

• London
• Remote
• Director

Medically responsible at trial level across preparation, conduct and reporting phases, providing medical expertise and oversight from Trial Design Outline to Clinical Trial Report. Dedicated to a single sponsor in the EMEA region, the role involves authoring high-quality clinical trial protocols, co-authoring Clinical Quality Monitoring plans, integrating medically relevant data into risk-based quality management, and performing ongoing reviews of medical data.

• London
• On-site
• Entry level
• Permanent

Contributes to the design and execution of cellular and biochemical assays, including arrayed CRISPR perturbation screens in established cell models, and maintains primary and immortalised mammalian cell lines with sample tracking and QC. Runs phenotypic readouts such as flow cytometry, RT-qPCR and ELISA, performs data analysis and quality assurance, and reports outcomes to cross-functional project teams. Based in London wet labs within a matrixed TechBio environment.

CRISPR · Flow Cytometry · RT-qPCR +3

• Cambridge
• Hybrid · 3 days in office
• Lead · manages people
• Permanent

Accountable to the Global Clinical Head for an indication-aligned cluster of late-phase Respiratory and Immunology studies, supervising Global Development Medical Directors and Scientist Directors. Leads cross-functional design, conduct, monitoring and data interpretation, represents the program at health authority interactions, and co-leads publication strategy.

• London
• Hybrid
• Mid-level
• Permanent

Join the Platform Team to design and scale Kubernetes-based hybrid compute clusters across private and public clouds, building core platform services and APIs. You will enhance CI/CD pipelines, monitoring, backup and disaster recovery, while partnering closely with Machine Learning and Data Science teams to support their computational needs.

Kubernetes · GitHub Actions · ArgoCD +3

• London
• Mid-level
• Permanent

Designs and implements generative models that learn intervention effects from single-cell perturbation and multiomic data, focusing on counterfactual prediction and experimental design. Works in interdisciplinary teams alongside experimental biologists to validate computational hypotheses and guide the highest-signal next experiments, with emphasis on causal coherence and real-world utility over benchmark fit.

• Exeter
• £21,805 pa
• Entry level
• Contract

Applies genetic clustering to severe mental illness traits to find biologically distinct risk components affecting obesity and type 2 diabetes, using GWAS data and population biobanks. Integrates single-cell multiomic datasets to map risk pathways to neuronal and glial cell types, with CRISPR-based functional work. Multidisciplinary training in statistical genetics, bioinformatics and functional genomics.

CRISPR · GWAS

• Hemel Hempstead
• Senior

Provides technical support and training to customers using mass spectrometry, LCMS and metabolomics platforms across EMEA. Delivers application optimisation, troubleshooting, presentations and product feedback to R&D, combining scientific expertise with customer engagement and up to 50-75% travel.

• Lisburn
• On-site
• Entry level
• Internship

A 12–14 month university placement for penultimate-year students, supporting the Statistical Programming group on clinical trials. Day to day you produce analysis and submission datasets, statistical tables, graphs and data listings using SAS, while learning about the pharmaceutical industry, clinical trial conduct and good clinical practice within a global project team.

SAS · R · MATLAB +1

• Ireland

Regional Laboratory Manager – DublinRandox are a world leader in diagnostics for clinical healthcare, toxicology, and food security. Our expertise and product portfolio have assisted laboratories across the world in improving health and saving lives. Our global success is a…

• Harrow
• Remote
• Senior

Monitors clinical trial sites across the UK as the sole point of contact, conducting qualification, initiation, monitoring and termination visits and producing visit reports. Manages site quality, regulatory documentation and drug accountability while developing recruitment strategies to meet enrolment timelines. Fully decentralised role with less travel and a lower protocol load than industry peers.

Clinical Trial Management System · Electronic Document Management System · Excel +1

• Harrow
• Remote
• Mid-level

Independently leads statistical aspects of low-to-moderate complexity clinical trials, developing complex analysis strategies and executing them with SAS or R. Reviews analysis datasets, quality-controls statistical deliverables, and contributes to trial design, analysis plans, and regulatory submissions. Works within global cross-functional teams, liaising with clients on data analysis, scope, and budget.

SAS · R