Medical Technology Jobs

196 jobs for “Clinical Research Associate”

Results

Bluetree logo

Bluetree · 11–50 people

Senior Regulatory Affairs & Quality Manager

  • Cambridge
  • Hybrid · 2 days in office
  • £65,000 – £80,000 pa
  • Senior
  • Permanent

Lead regulatory strategy for a cardiology device company expanding into the US, UK, EU and Middle East, owning FDA, CE and UKCA submissions from Class I to Class II/III. Drive an audit-ready QMS (ISO 13485, 21 CFR Part 820, ISO 14971) and advise senior leadership on regulation, quality and clinical governance, working directly with the FDA, MHRA and notified bodies.

FDA · MHRA · UKCA +2

Featured 3 weeks ago

University of Sheffield

Research Associate in Biomedical Engineering

  • Sheffield
  • £39,560 – £48,337 pa
  • Entry level
  • Contract

Lead the design, assembly and clinical validation of a novel dialyser prototype, testing it with blood-mimicking fluids and human blood to assess cleaning efficiency, clotting risk and biocompatibility. Work within the Thermofluids Group alongside experts in engineering, medicine and Sheffield Teaching Hospitals, collaborating with two other Research Associates on simulations and fluid dynamics.

6 days ago

University of Bristol

Research Associate in Cardiovascular ncRNA Therapeutics

  • 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

Last week

Healthium Clinics

Regulatory Affairs Associate / Compliance Officer

  • Henley-on-Thames
  • £32,000 – £38,000 pa
  • Mid-level
  • Permanent

Support regulatory affairs and compliance across healthcare, digital health and medical-device activity. Maintain the Quality Management System, medical-device technical documentation, risk registers and audit actions, while coordinating evidence for tenders, CQC inspections and information governance. Acts as a link between clinical, technical and commercial teams.

ISO 13485 · ISO 14971 · IEC 62304 +7

Last month

Jazz Pharmaceuticals

Associate Director, Central Monitoring

  • 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

Last week

Jazz Pharmaceuticals

Associate Director, Central Monitoring

  • 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

Last week

Get new Clinical Research Associate roles by email. One email a morning when new roles match. Stop any time.

SoCode

Senior Product Manager

  • 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

Last week

Medtronic · 10000+ people · Public

Associate Technical Consultant

  • Cambridge
  • £36,000 – £54,000 pa
  • Entry level

A 12-month structured development programme in cardiac electrophysiology, training early-career professionals to support Affera mapping and ablation procedures in hospital cath labs. Field-based across the Midlands, it combines clinical education, mentorship and hands-on procedure support, with progression into a Technical Consultant role on completion.

Affera Mapping Technology

Last week
NHS Professionals logo

NHS Professionals · 1001–5000 people · Public

Pharmacy technician for Clinical Trials

  • 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

Clearance required Last week
Johnson & Johnson MedTech logo

Johnson & Johnson MedTech · 10000+ people · Public

Associate Technical Specialist | Electrophysiology

  • Maidenhead
  • Entry level

Field-based clinical and technical support role covering the Electrophysiology portfolio, spending 80%+ of time with customers supporting AF and CTI procedures and building CARTO hardware, software and HD mapping expertise. Works within a POD alongside Technical Specialists and Sales to drive case coverage, customer education and account growth while completing a structured training pathway.

CARTO · CARTOSOUND · Axonify +1

3 days ago
NHS Professionals logo

NHS Professionals · 1001–5000 people · Public

Biomedical Scientist

  • Worcester
  • On-site
  • £20 pa
  • Mid-level
  • Contract · Part time

Perform biochemical analyses on patient samples using manual and automated techniques, maintain and QC point-of-care testing equipment, and authorise results for electronic reporting to wards. The role includes out-of-hours rota cover, giving technical advice to clinical staff, and supporting quality management within a hospital Clinical Biochemistry service.

POCT

Today
Newton Colmore logo

Newton Colmore · 11–50 people

PhD Level Ultrasound Technology Consultant - Cambridge

  • Cambridge
  • Entry level

Drive development of next-generation surgical and interventional devices, applying ultrasound expertise across the full innovation pathway from feasibility studies to market preparation. Work spans robotic surgical platforms and intelligent instruments with integrated sensing, collaborating with partner organisations on technical strategy. Suits a PhD-level ultrasound specialist keen to shape projects and influence technical direction.

EN 60601

3 weeks ago
Johnson & Johnson MedTech logo

Johnson & Johnson MedTech · 10000+ people · Public

Sales Specialist |Mentor| North East Region

  • Maidenhead

Field-based sales role covering the North East region, growing the breast implant and reconstruction device business across public and private secondary care. You own clinical and commercial relationships with plastic and oncoplastic breast surgeons, build account business plans, and lead customer education with support from marketing and professional education teams.

Oracle Customer Data Management (CDM)

2 days ago
Philips logo

Philips · 10000+ people · Public

Clinical Scientist MR

  • United Kingdom - Remote Based
  • Remote
  • £49,140 – £77,220 pa
  • Mid-level

Supports MRI research collaborations across multiple UK&I partner sites as part of a Europe-wide Clinical Science team. Runs Philips MR scanners, programs pulse sequences and reconstruction, provides first-line scientific support to customers, and contributes to academic papers and clinical training. Field-based role with national and occasional international travel.

Philips MR Scanners

2 days ago

SoCode

Clinical Data Manager

  • 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

Last month

Clearline Recruitment Ltd

Clinical Study Manager

  • 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.

3 weeks ago

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