Live clinical research associate roles plus reconciled 2026 salary data by region.
Remote
IQVIA LLC is seeking a Clinical Research Monitor to oversee site monitoring and management, ensuring studies are conducted per protocol and…
Remote
Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully…
Lancashire
To conduct research in NIHR portfolio studies in the priority area of: Cardiovascular disease.
Sutton
The West Wing Clinical Research Centre at The Royal Marsden NHS Foundation Trust in Sutton is seeking an Administrative Assistant/ Scheduler/…
Remote
Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator I to conduct and manage clinical trials in line with the study protocol…
Remote
Velocity Clinical Research, Inc. seeks a candidate to support recruitment plans, pre-screening, and tracking of potential clinical trial participants.
London
Montu UK is seeking a Clinical Operations Coordinator to optimise clinician capacity and rota planning.
London
12-Month Regulatory Affairs CMC Student Placement offering exposure to regulatory strategy, submissions management, health authority engagement, and…
London
MSD invites applications for a 12-month Regulatory Affairs CMC student placement in London.
London
IQVIA LLC seeks a Senior Project Manager to lead global clinical trials, delivering strategic leadership for complex studies and partnering with…
London
Relocation Support: This role is based in London, United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.
London
Novartis is seeking a Study & Site Operations (SSO) Cluster Head in London to lead the delivery of complex clinical trials across global programs.
Slough
Are you an experienced Pharmacovigilance Systems professional who enjoys bridging the gap between business operations, technology, and patient safety?
Aylesford
An international ingredients and nutrition solutions company is looking for a Regulatory Affairs Specialist to provide regulatory expertise across…
Manchester
Tigermed is seeking an experienced Clinical Research Associate in Manchester to oversee site management, training, and documentation across trials…
London
This range is provided by Metric Bio. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Redditch
W Talent are delighted to be partnering with an established manufacturing business to recruit a Regulatory Affairs Specialist.
Manchester
Arxada is looking for a Regulatory Affairs Specialist based in Manchester, UK.
Aylesford
An exciting opportunity has arisen for a Regulatory Affairs Specialist to join a growing and collaborative quality team within an international…
Are you a natural leader and able to inspire others? Do you have the drive, enthusiasm and talent to lead others?
London
Bartle Bogle Hegarty (BBH) in London seeks a meticulous Senior Medical Writer with promotional healthcare agency experience to elevate complex…
An outstanding opportunity has arisen within a leading, innovation-driven pharmaceutical company dedicated to delivering value-based…
Hull and East Yorkshire
Science Recruitment UK is partnering with an East Yorkshire manufacturer to recruit a Technical and Regulatory Associate.
Nottingham
R&D Partners in the United Kingdom is seeking a Regulatory Affairs Manager to lead a team of regulatory experts and drive strategic initiatives for…
London
Access Partnership is the frontier consultancy getting innovation into market faster across technology, AI, Space and Health.
Premier Research is seeking a Director of Study Start Up in the United Kingdom to lead SSU teams and drive timelines in the region.
Thatcham
Fortrea is seeking a Manager II, Clinical Operations to lead a team of clinical research professionals across the UK/IRE.
Oxford
In this role, you will assist in the design and set-up of clinical trials within a multidisciplinary team including (but not limited to) the Chief…
Bradley Stoke
If you’ve worn a pair of glasses, we’ve already met.
Metropolitan Borough of Solihull
Working across both established and emerging product categories, you’ll keep up to date on changing regulations, provide expert guidance to…
London
A leading healthcare firm in London is seeking an Associate Director of Project Management to lead project management teams and oversee Expanded…
High Wycombe
Apply locations UK - High Wycombe, Buckinghamshire time type Full time posted on Posted 30+ Days Ago job requisition id JR
This range is provided by RBW Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Reading
Kenvue is recruiting for Regulatory Affairs Industrial Placements in the UK, based at Reading HQ.
Cambridge
Newton Colmore in Cambridge is seeking a Regulatory Affairs Engineer to support medical devices across development projects.
London
TOGL(Holdings)Limited is a diagnostics company focused on GI tract diseases, seeking a Regulatory Manager to drive regulatory strategy and…
Oxford
The Ellison Institute of Technology (EIT) is seeking a Clinical Operations, Partnership Manager to join the Commercial Projects team in the Legal…
London
Amgen seeks an EU Regulatory Affairs Manager to drive submissions for clinical trials and marketed products from a regulatory perspective within the…
London
If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do.
Wantage
The role reports to the Head of Materials Compliance, supporting the delivery of the broader EMEA regulatory vision and the mitigation of regional…
Oxford
At the Ellison Institute of Technology (EIT), we’re on a mission to translate scientific discovery into real world impact.
Boston
At BioTalent, we are working with a client exclusively to fill their RA Specialist position.
This range is provided by Select Pharma Recruitment.
A leading clinical research firm in the United Kingdom seeks an experienced project manager to oversee end-to-end delivery of clinical studies.
A leading global CRO is seeking a Vice President of Clinical Operations for their Cardiovascular Business Unit.
A leading biotech firm in the UK is seeking a Regulatory Affairs Director to transform the treatment of neuropsychiatric disorders by supporting…
Cambridge
A pioneering life sciences organization in Cambridge is seeking a Regulatory Affairs Manager to lead regulatory strategy and execution throughout…
London
A leading pharmaceutical company in London is seeking a Data Information Model Developer to organize and structure scientific data for R&D teams.
Marlow
Amicus Therapeutics is a global, patient-dedicated biotechnology company focused on discovering, developing, and delivering high-quality medicines…
A leading provider of pharmacovigilance solutions in the United Kingdom is seeking a Consulting Technology Project Manager.
Churwell
Johnson & Johnson invites applications for a Regulatory Affairs Placement Student in Leeds.
Milton Keynes
Are you immediately available and looking for a new opportunity with a global food manufacturer?
London
Teya was founded on a simple belief: local businesses deserve better.
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Reading
IQVIA is seeking a Senior Clinical Research Associate (cFSP sponsor-dedicated) in Reading to monitor sites and manage study data per protocol and GCP.
Leeds
Do you have experience leading data management activities across early phase studies?
London
The Institute of Cancer Research, together with the Royal Marsden NHS Foundation Trust, invites applications for a Clinical Research Fellow in…
London
Our Future Health is seeking a Research Access Reviewer to lead scientific and technical reviews of proposals for data, samples and participant…
London
Cpl Group, based in Holborn, London, seeks an experienced trials professional to set up and support a high-quality clinical trial at the CCTU.
| Region | Salary range (median) |
|---|---|
| London (indicative) no live adverts yet: baseline range |
£45,000 – £70,000 (midpoint £57,500) |
| South East (indicative) no live adverts yet: baseline range |
£42,000 – £65,000 (midpoint £53,500) |
| Midlands (indicative) no live adverts yet: baseline range |
£38,000 – £58,000 (midpoint £48,000) |
| North West (indicative) no live adverts yet: baseline range |
£38,000 – £58,000 (midpoint £48,000) |
| Scotland (indicative) no live adverts yet: baseline range |
£38,000 – £58,000 (midpoint £48,000) |
| Yorkshire (indicative) no live adverts yet: baseline range |
£36,000 – £55,000 (midpoint £45,500) |
Methodology: medians reconcile live advertised UK salaries for this role and region; 25th–75th percentiles are shown only where at least 5 live salaried listings back them. They are measured or omitted, never interpolated. Rows marked indicative are anchored to our curated 2026 baseline ranges until enough live data accrues. Listings advertising an implausible annual figure (a mislabelled hourly or daily rate) are excluded rather than converted, because converting one means guessing the hours behind it.
Indicatively £38,000–£58,000, senior CRAs £55,000–£70,000; clinical project managers £65,000+.
Usually via a clinical trial assistant or study coordinator role plus a life-science degree; ICH-GCP training is essential.
Right to work, references, GCP certification and a driving licence for monitoring roles.
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