Medical Technology Jobs

• London
• Senior

Own the technical delivery of AI initiatives end to end, taking HealthHero's flagship Clinical Brain from prototype to production. The role involves designing an AI layer that interacts with deterministic components of a Class II medical device, combining NLP, LLMs and machine learning, and building rigorous evaluation pipelines with golden datasets, mixtures of evaluators and human-in-the-loop clinician review.

AWS · GCP · Azure +7

• London
• Senior

Owns end-to-end delivery of AI initiatives, starting with the Clinical Brain, a Class II medical device combining an AI layer with deterministic components. Involves NLP, LLMs, knowledge graphs, rigorous evaluation with golden datasets and clinician review, plus LLMOps and regulated documentation alongside clinical and compliance leads.

Neo4j · Cypher · GraphRAG +5

• Edinburgh
• On-site
• £76,800 – £115,200 pa
• Senior

Own the end-to-end data lifecycle for an AI and algorithm R&D team, from clinical study data collection through validation trials. Design and manage scalable infrastructure across clinical trials, sensor platforms and HPC environments, building ETL/ELT pipelines and data tooling in Python and SQL while shaping data architecture standards.

Python · SQL · C++ +3

• London
• Hybrid · 2 days in office
• £76,800 – £115,200 pa
• Senior

Designs, builds and maintains AWS and on-prem infrastructure used by ML engineers, data scientists and product teams, with a strong focus on Kubernetes, GitOps, Terraform and Docker. The role sits in the Surgical AI Centre of Excellence, supporting an MLOps platform for connected operating-room products, and requires two days a week in London.

Kubernetes · Helm · AWS +5

• Beerse, Belgium
• Senior

Combines rigorous statistical thinking with modern AI to build validated, reusable AI-enabled statistical solutions for pharmaceutical research and manufacturing. Hands-on work spans Python services, LLMs, RAG, agentic workflows, APIs and MCP, ensuring statistical integrity, reproducibility and traceability in a regulated environment.

Python · R · SQL +7

• Leiden, Netherlands
• Senior

Develops trustworthy, validated AI-enabled statistical solutions for pharmaceutical research and manufacturing, working at the intersection of biostatistics, AI and scientific software development. Builds Python services, connects R and Python tools via APIs and MCP, and creates agentic workflows using LLMs and RAG. Ensures statistical integrity, reproducibility and governance in a regulated environment.

Python · R · SQL +7

• Guildford
• £48,337 – £70,878 pa
• Senior
• Permanent

Develop an independent, externally funded research programme as a Principal Investigator, applying AI and data science to human, animal and environmental health data within a One Health framework. Collaborate across medicine, veterinary science, computer science and engineering, secure UK and international funding, publish high-quality work, and teach AI and data science at undergraduate and postgraduate level.

• Hanoi, Vietnam
• Permanent

Research-focused faculty role in precision medicine and health technology, working with research centres in the Innovation in Health Sciences cluster. Involves leading AI-assisted research on wellness, disease prevention and early detection, teaching accredited undergraduate and graduate curricula, supervising students, and contributing to university service and commercialisation.

• London
• Hybrid
• Mid-level · manages people
• Permanent

Own the regulatory strategy for a venture-backed medical device company preparing its FDA 510(k) submission. Lead the 510(k) through review, act as primary FDA contact, coordinate test evidence across engineering and CROs, and build US post-market processes while shaping UK and EU MDR strategy.

GUDID

• Oxford
• On-site
• Permanent

Contribute directly to research projects combining molecular biology, RNA biology, epigenomics, epitranscriptomics, synthetic biology and AI/ML-driven design methods. Work closely with internal Machine Learning, Biomolecule Synthesis and wider research groups on integrated, multidisciplinary research across the company.

• Welwyn Garden City
• Hybrid · 3 days in office
• £450 – £500 ph
• Lead
• Contract

Coordinate clinical study start-up, site activation and UK regulatory submissions, managing trial amendments, essential documentation, site contracts, budgets and payment processes. Work with R&D, clinical sites, global study teams and CROs to ensure ICH-GCP compliance, using UK systems such as IRAS, CPMS, iCT and ARSAC. Practical UK study set-up experience is essential.

IRAS · CPMS · iCT +1

• Welwyn Garden City
• £377 – £500 ph
• Mid-level
• Contract

Coordinate early-phase clinical trials within a pharmaceutical Clinical Operations team, covering study start-up, feasibility, timelines, recruitment and vendor oversight. Maintain TMF documentation, risk logs and regulatory compliance under ICH-GCP while working with Data Management, Regulatory Affairs and external partners.

Trial Master Files · Microsoft Office

• Cambridge
• Hybrid · 2 days in office
• £48,000 pa
• Permanent

Own data management across a portfolio of clinical studies, from setup through database lock and final data transfer, acting as the primary client contact for data quality and delivery. Configure and test data transfers, write production code, produce ETL-based reports, and maintain GCP documentation, with scope to improve SOPs and explore AI tools.

Python · SQL · SAS +2

• Cambridge
• Remote
• Director · manages people

Leads Jazz's central monitoring capability within Global Clinical Development Operations, defining and interpreting portfolio-level key risk indicators and statistical signals to drive risk-proportionate monitoring strategy at site, study and CRA level. Partners with Trial Risk Management, Site Monitoring, Data Management and Biostatistics, owns RBQM technology platforms, and manages a team of central monitoring analysts.

CTMS · EDC Systems · RBQM Systems +2

• London
• Remote
• Director · manages people

Leads Jazz's central monitoring capability within Global Clinical Development Operations, defining and interpreting portfolio-level key risk indicators and statistical signals to drive risk-proportionate changes in site, study and CRA monitoring strategy. Partners with Trial Risk Management, Data Management and Biostatistics, owns RBQM technology platforms, and manages a team of central monitoring analysts while championing AI-enabled risk detection.

CTMS · EDC