Medical Technology Jobs

• 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

• 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

• 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.

• High Wycombe
• Entry level
• Internship

A 12-month industry placement within the Integrated Data Analytics and Reporting function, specifically Clinical and Statistical Programming. The student applies SAS, R and Python to analyse trial data, build automation and AI-driven tools, and document solutions across disease areas, working alongside programming experts in a pharmaceutical research department.

SAS · R · Python +4

• Maidenhead
• Entry level
• Internship

A 12-month industry placement within the Integrated Data Analytics and Reporting function, specifically Clinical and Statistical Programming. The student applies SAS, R, Python, RPA and Power Automate to analyse trial data, build automation and AI-driven tools, and document solutions across disease areas. Distinct for combining hands-on clinical research analysis with emerging AI technologies.

SAS · R · Python +4

• United Kingdom, YY9 9YY
• Remote
• Mid-level

Provides day-to-day medical oversight for one or more clinical trials, ensuring patient safety, data integrity and protocol compliance. Reviews and assesses AEs and SAEs, supports safety signal detection with Pharmacovigilance, and advises investigators on eligibility and dosing. Works cross-functionally with Clinical Operations, Data Management, Biostatistics and Regulatory Affairs, and contributes to CSRs and regulatory submissions.

Data Safety Monitoring Boards

• 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

• Birmingham
• Hybrid
• Mid-level

Builds and runs an AI-enabled competitive intelligence platform for the pharmaceutical market, working end to end from PostgreSQL and Python APIs through to React and TypeScript interfaces. Sits in a small Birmingham-based team, developing data-rich workflows for consulting users and gathering their feedback directly.

React · TypeScript · Python +4

• 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.

• Bristol
• £30,000 – £35,000 pa
• Entry level

You will demonstrate, install, train and support an advanced range of radiotherapy hardware and software, including patient and machine QA devices, AI tumour-mapping software, SGRT and patient positioning equipment. Working with Medical Physicists, Dosimetry and Radiotherapy teams across Southern England, you average one to two nights away per week while building clinical relationships.

SGRT

• Guildford
• £30,000 – £35,000 pa
• Entry level

You'll demonstrate, install, train and support an advanced range of radiotherapy hardware and software, including patient and machine QA devices, AI tumour-mapping software, an SGRT system, and patient positioning devices. Covering a Southern England territory with 1-2 nights away per week, you'll build relationships with Medical Physicists, Radiotherapy and Dosimetry teams, supported by experienced colleagues who train and mentor you.

SGRT

• Birmingham
• Entry level
• Contract

Fully funded PhD studentship in Chemical and Biomedical Engineering, joining the Advanced Nano Materials, Structures and Applications group. The research develops miniaturised point-of-care diagnostic devices, engineering intelligent spectroscopic techniques to non-invasively detect and quantify disease, with clinical validation and applications in monitoring cellular and tissue responses to therapy.

• London
• Hybrid · 2 days in office
• £87,600 – £131,400 pa
• Lead

Owns the multi-year product vision and platform strategy for an edge-compute and connectivity foundation used in operating rooms, spanning video, data movement, fleet operations and real-time AI workloads. Works with engineering, clinical and commercial partners in a regulated environment, requiring at least two days a week in the London office.

Touch Surgery · Touch Surgery Aide

• 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

• 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