Medical Technology Jobs

• Leeds
• Hybrid
• Entry level
• Internship

Supports a Clinical Operations team in the day-to-day coordination of clinical studies, maintaining the Trial Master File (TMF/eTMF), tracking activities in CTMS, generating reports and distributing study supplies and regulatory documentation. A student placement offering hands-on exposure to clinical research processes and systems, working with study teams, project managers and site managers. Based in Leeds with flexibility to work remotely, though onsite working is preferred.

Microsoft Office · Microsoft Excel · Microsoft Word +4

• Leeds
• Entry level
• Internship

A 12-month student placement in the clinical research department, supporting international trials of medical technology products. The role involves administrative tracking and monitoring of high-profile studies, maintaining essential documents, data collection, and coordinating logistics from setup to completion, with exposure to cutting-edge clinical trials.

Microsoft Excel · Microsoft Word · Microsoft PowerPoint

• Welwyn Garden City
• Hybrid · 2–3 days in office
• £339 – £500 pd
• Lead
• Contract

Country and site-facing role coordinating UK clinical trial start-up through to site activation, managing regulatory submissions, approvals and amendments with the HRA, Ethics and MHRA. Involves liaising with NHS R&D departments, clinical sites and CROs, negotiating site contracts, budgets and costing templates, and tracking timelines and regulatory milestones. Requires recent hands-on UK study start-up experience and knowledge of IRAS, CPMS, iCT and ARSAC.

IRAS · CPMS · iCT +4

• Welwyn Garden City
• Hybrid · 3 days in office
• £377 – £550 pd
• Mid-level
• Contract

Operational delivery of early-phase clinical trials, coordinating multi-country study activities, timelines and site start-up while managing vendors, CROs and study documentation such as Trial Master Files. Works closely with international study teams and cross-functional groups to ensure ICH-GCP compliance, manage risks and improve study processes.

• UK - Field
• Hybrid
• Senior

Leads complex, S+N-sponsored clinical studies from start-up to close-out, acting as project leader within cross-functional teams spanning biostatistics, data management, regulatory affairs and vendors. Develops protocols, monitoring plans and consents, oversees vendors and site management, manages study budgets, and ensures GCP and ISO 14155 compliance. Also trains junior clinical study management staff.

ISO 14155 · ISO 9001 · ICH-GCP

• 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

• 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

• 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

• 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

• Nottingham
• On-site
• £16 ph
• Lead · manages people
• Temporary

Lead and coordinate technical aspects of clinical trial activities across QMC and City Hospital, supervising dispensing, accountability records for IMPs/NIMPs, and stock control. Manage clinical trials technical and support staff, liaise with sponsors and research teams, and prepare for sponsor audits and MHRA inspections.

ChemoCare

• Bristol
• On-site
• £40,704 – £45,641 pa
• Entry level
• Contract

A 9-month post-doctoral position in the Laboratory of Cardiovascular Pathology at Bristol Medical School, working under Professor Jason Johnson. The project evaluates non-coding RNAs as therapeutics and diagnostics for atherosclerotic cardiovascular disease, involving pharmacodynamic and pharmacokinetic assessment, human tissue and ex vivo bio-reactor work, next-generation sequencing and bioinformatic analysis, plus day-to-day project management and liaison with academic and industrial partners.

Microsoft Word · PowerPoint

• 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

• Cambridgeshire
• Hybrid
• Senior
• Permanent

Owns product strategy, commercial business cases and portfolio development for digital clinical trial technologies, spanning eCOA, digital biomarkers and patient data collection. Works across Product, Engineering, Science, Regulatory and Commercial teams, leading customer discovery, market sizing, financial modelling and go-to-market planning in a regulated life sciences environment.

eCOA