Regulatory specialist Work, Jobs in Loughton, Ess (with Salaries)

Clinical Trials Coordinator
University College London —London
- £43,981 a year
- Full-time
- Hybrid work
5d
Research Regulatory Facilitator
Imperial College London —White City
- £48,246 - £58,318 a year
- Full-time
- University
- Time management
- Annual leave
4d
Clinical Trials Coordinator part time 0.5 FTE
University College London —London
- £21,990.50 a year
- Part-time
- Hybrid work
5d
Nutrition Specialist (Global Regulatory & Corporate Affairs)
Oatly AB —London
- Part-time
- Hybrid work
- English
- Master's degree
- Travel
Quick apply
FSQRN Data & Analytics Specialist
Starbucks —London
- Full-time
- Analysis skills
18h
Cancer Referral Specialist
Lloyds Clinical —Harlow
- £48,000 a year
- Hybrid work
- IT
- Communication skills
- Annual leave
- Employee assistance programme
Quick apply
Clinical Evaluation Specialist
Scarlet —London
- £75,000 - £90,000 a year
- Full-time
- Nursing
- Sales
- Patient care
Medical Information Specialist - Afterhours
EVERSANA —London
- Weekend availability
- Remote
- Microsoft Word
- Computer literacy
- English
Quick apply
7d
Regulatory Data Specialist - Contract Role 12 months
Synthomer (UK) Limited —Harlow
- Hybrid work
- Continuous improvement
- Employee assistance programme
Quick apply
5d
Regulatory Compensation Specialist
Bank of America —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Employee assistance programme
Research Analyst
Infopro Digital Services Limited —London
- Full-time
- Hybrid work
- Analysis skills
- Bachelor's degree
- Financial services
- Annual leave
- Employee assistance programme
Quick apply
Regulatory Specialist - Commodity Chemicals
Synthomer (UK) Limited —Harlow
- Databases
- Continuous improvement
- Employee assistance programme
Quick apply
6d
Quality Assurance Specialist
MSD —London
- Full-time
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Quality control
6d
Device Specialist
Scarlet —London
- £75,000 - £85,000 a year
- Full-time
- Writing skills
- Engineering
- Bachelor's degree
12d
Global Benefits Senior Specialist
Boston Consulting Group —London
- Full-time
- Microsoft Excel
- Data analysis skills
- Analysis skills
Compliance Reporting Specialist
Hampshire Trust Bank —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
Quick apply
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- English
Quick apply
Regulatory Change Implementation Specialist - 2026
Suade —London
- £50,000 - £75,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- English
- Bachelor's degree
- Annual leave
- Work from home
Quick apply
Data Compliance Specialist
SIX Group AG —London
- Call to connect
- Remote
- Spanish
- Microsoft Excel
- Sales
Quality and Regulatory Manager
Advanced Healthcare Technology Ltd —Waltham Cross
- £50,000 - £60,000 a year
- Full-time
- No degree
- Organisational skills
- In-person
- Free parking
Quick apply

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regulatory specialist jobs near loughton, ess

Clinical Trials Coordinator

University College London -
London

Apply Now

Job details

Full-time | Fixed term contract
£43,981 a year
5 days ago

Qualifications

Healthcare research operations
Clinical research

Full job description

Ref Number

B02-11005

Professional Expertise

Research and Research Support

Department

School of Life & Medical Sciences (B02)

Location

London

Working Pattern

Full time

Salary

See advert text

Contract Type

Fixed-term

Working Type

Hybrid

Available for Secondment

Closing Date

13-Aug-2026

About us

The Department of Translational Neuroscience and Stroke (DTNS) is a hub for clinical and research excellence. DTNS is home to a collaboration of interlinked neurological research areas, each one focused on advancing translational scientific knowledge to further patient recovery and management and educating through teaching and academic supervision.

The UCL Stroke Research Centre is an internationally recognised leader in the field of clinical stroke research. We are dedicated to doing cutting-edge research to improve the care of people with stroke. We work in close partnership with UCL Hospitals NHS Foundation Trust Comprehensive Stroke Service, which is home to an Emergency Stroke Unit, Hyperacute Stroke Unit and Research Centre, and an Acute Stroke Unit. Our service covers a large catchment population for referrals of about 1.6 million people and sees specialist referrals from the whole of the UK.

About the role

The Stroke Research Centre at the UCL Queen Square Institute of Neurology is seeking a Clinical Trials Coordinator to support the DOAC International Thrombolysis (DO-IT) study. This is an exciting opportunity to join a world-leading centre for stroke research and contribute to an international clinical trial aimed at improving outcomes for patients with stroke.

Working with the other Clinical Trials Coordinator, you will be responsible for coordinating the DO-IT study and other clinical trials within the Stroke Research Centre. This includes managing regulatory documentation, liaising with sponsors and collaborators, organising trial visits, and ensuring compliance with UK and international research regulations.

The post is available from 01 September 2026 and is funded by the British Heart Foundation until 31 August 2028 in the first instance.

This role is eligible for hybrid working with a minimum of 60% of time on site.

If you need reasonable adjustments or a more accessible format to apply for this job online, or have any queries regarding the application process, please contact the Institute of Neurology HR Team ([email protected]).

For informal enquiries about the role, please contact Professor David Werring ([email protected]).

For a full job description please visit UCL’s online recruitment portal (https://www.ucl.ac.uk/work-at-ucl/search-ucl-jobs) and search using vacancy reference B02-11005. To apply, please upload a current CV, complete the online application form, and use the supporting statement section or upload a cover letter to outline how you meet the essential and desirable criteria for the role. Please do not upload any additional attachments as these will not be considered by the selection panel.

About you

You will have significant experience in clinical trials work in a medical research environment, knowledge of data protection legislation, experience in data management with the ability to handle sensitive data appropriately. Experience of working in clinical research and managing or coordinating a project is essential, as is experience of setting up and coordinating studies, experience of budget preparation/finance management, and an understanding of ethical issues surrounding research and patients.

What we offer

Starting salary offered at £43,981 per annum, including London Allowance.

As well as the exciting opportunities this role presents, we also offer great benefits, visit https://www.ucl.ac.uk/work-at-ucl/reward-and-benefits to find out more.

This appointment is subject to UCL Terms and Conditions of Service for Research and Professional Services Staff. Please visit https://www.ucl.ac.uk/human-resources/conditions-service-research-teaching-and-professional-services-staff for more information.

Our commitment to Equality, Diversity and Inclusion

As London’s Global University, we know diversity fosters creativity and innovation, and we want our community to represent the diversity of the world’s talent. 12% of Institute staff are actively working on EDI initiatives; visit https://www.ucl.ac.uk/ion/equality-diversity-inclusion for more information about what we’re doing. We therefore particularly encourage applications from candidates who are likely to be underrepresented in UCL’s workforce; these include people from Black, Asian and ethnic minority backgrounds, disabled people, LGBTQI+ and gender diverse people in all roles, and women in Grade 9 and 10 roles.

Apply Now

Refine Your Search

regulatory specialist jobs in loughton, ess

Clinical Trials Coordinator

Research Regulatory Facilitator

Clinical Trials Coordinator part time 0.5 FTE

Nutrition Specialist (Global Regulatory & Corporate Affairs)

FSQRN Data & Analytics Specialist

Cancer Referral Specialist

Clinical Evaluation Specialist

Medical Information Specialist - Afterhours

Regulatory Data Specialist - Contract Role 12 months

Regulatory Compensation Specialist

Research Analyst

Regulatory Specialist - Commodity Chemicals

Quality Assurance Specialist

Device Specialist

Global Benefits Senior Specialist

Compliance Reporting Specialist

Medical Information Specialist - US Hours

Regulatory Change Implementation Specialist - 2026

Data Compliance Specialist

Quality and Regulatory Manager

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