206 jobs within 10 miles of London
Acts as a QA liaison between clinical trial teams and third parties, providing expert support through due diligence, qualification, governance and ongoing monitoring. Focuses on technology-enabled vendors such as digital health tools, medical devices and AI, covering risk assessment, audit support, inspection readiness and escalation of quality issues.
DHT · SaMD · SaaS +1
Leads statistical programming strategy across multiple trials or a full program, acting as Trial, Lead or Program Programmer and coordinating internal and external programmers. Develops and validates CDISC-compliant datasets and outputs for CSRs, regulatory submissions and safety reports, using R, SAS or Python, Git-based version control and reproducible workflows. Also shapes standards, templates and governance, with hybrid working from London.
R · SAS · Python +4
Isomorphic Labs · 201–500 people · Series A
Join the Compute Infrastructure team to keep a planet-scale GPU accelerator fleet healthy and efficient. You'll build observability and telemetry pipelines, automate recovery, hunt compute waste, and optimise accelerator utilisation for large-scale training and inference, working closely with ML infrastructure and research teams.
GCP · Kubernetes · Nvidia GPU +1
Isomorphic Labs · 201–500 people · Series A
Lead medicinal chemistry strategy across drug discovery programmes, from hit identification through lead optimisation to candidate nomination, while working hands-on as an individual contributor. Partner closely with AI/ML platform teams to shape predictive models, manage CRO resources and KPIs, and represent the company externally with collaborators.
AlphaFold
IQVIA
Supports UK clinical trial start-up by collecting and reviewing site and regulatory documentation, preparing submission packages, and coordinating Informed Consent Form adaptations. Liaises with investigative sites and internal study teams to resolve outstanding documents and track progress against milestones, ensuring ICH-GCP and local regulatory compliance.
Imperial College London
Supports the production and characterisation of recombinant proteins for molecular glue discovery, focusing on expression, purification and characterisation using mammalian cell systems. Contributes to biochemical or biophysical assay development and helps run the laboratory day to day, including equipment upkeep, consumables and waste disposal, within a multidisciplinary chemical biology and proteomics team.
HEK293 · Expi293 · Agilent Measurement Suite
AstraZeneca · 10000+ people · Public
Deliver and maintain UK competitive licences, lead regulatory strategy for new initiatives, and ensure compliance across defined products and projects. Provide local regulatory expertise for clinical trial approvals, lifecycle submissions and MHRA interactions, contributing to cross-functional teams and study feasibility work.
Veeva · AI
UCL
Develops and leads an AI-driven research programme in biomolecular design and molecular interactions, spanning protein-ligand, protein-protein and protein-nucleic acid systems. Combines structural biology, biophysics, quantitative biology and machine learning, while teaching computational biology and biomolecular design at undergraduate and postgraduate level, including a new MRes in AI for Bioscience.
Genomics
Owns the transition from discovery to delivery on Mystra, a scientific data platform, breaking strategic initiatives into well-scoped epics and features. Works with scientific SMEs, data services, engineering and design to ensure requirements are scientifically valid and technically sound, running kick-offs and bi-weekly check-ins. Requires fluency with genomic data such as GWAS papers, p-values and effect sizes.
Mystra
Basecamp Research
Lead research on the capabilities and risks of biological AI systems, designing evaluations, red-teaming studies and threat models, and developing safeguards across training, model behaviour and access. Work within the frontier model team with access to proprietary genomic data and biological expertise, shaping research priorities and publishing where appropriate.
EDEN · BaseData
IQVIA
Monitors Phase I-IV clinical trials across UK sites, conducting evaluation, initiation, interim and close-out visits in line with GCP and sponsor requirements. Works closely with the Clinical Trial Manager and Lead CRA, handling source verification, eCRF/EDC data review, query resolution and site training. Requires oncology monitoring experience and involves travel plus mentoring of less experienced CRAs.
EDC · eCRF
Latent Labs
Architect novel generative models to design functional proteins, working in an interdisciplinary team of ML researchers, protein engineers and biologists. Split roughly 90% model building and 10% self-development, spanning data curation, evaluation metrics, prototyping, cloud training/inference and wet lab testing campaigns.
Francis Crick Institute
Supports research into how mice process odours to guide foraging behaviour, running behavioural experiments with freely moving animals and training them on olfactory tasks. The postholder also helps build and maintain data acquisition and analysis pipelines, keeps detailed experimental records, and presents findings at lab meetings. Based in a systems neuroscience group using electrophysiology, calcium imaging and computational modelling.
Francis Crick Institute
Investigates how protein machines remodel microtubules using cryo-electron microscopy, protein reconstitution and fluorescence microscopy. As an early member of a new lab, you will shape the research programme, establish experimental approaches and develop scientific independence while working closely with the group leader.
Cryo-EM
Ipsen
Leads global clinical data transparency and disclosure across registries and regulatory platforms such as CTIS, EMA Policy 0070 and Health Canada PRCI, acting as subject matter expert for assigned therapeutic areas. Manages vendor partnerships, FOI access requests, redaction and lay summary work, plus SOP governance, compliance reporting and audit readiness within Global Regulatory Affairs Excellence.
CTIS · ClinicalTrials.gov · EU Clinical Trial Register +3
