Clinical trial regulatory Work, Jobs in London, Eng (with Salaries)

Clinical Research Coordinator
SAVA —London
- Communication skills
Quick apply
1h
Clinical Trial Associate Manager
Galderma —London
- Hybrid work
- Project management
- Bachelor's degree
- Leadership
Clinical Research Assistant
Care One —West London
- £25,420.00 - £45,649.17 a year
- Full-time
- Patient monitoring
- Data analysis skills
- Analysis skills
Quick apply
10d
Clinical Research Associate, South East England
IQVIA —London
- Full-time
- Maintenance
- No degree
5d
Clinical Trials Manager
Imperial College London —London
- £46,614 - £56,345 a year
- Full-time
6d
Senior Clinical Trial Administrator
GE HEALTHCARE —Chalfont Saint Giles
- Travel
- Communication skills
7d
Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)
サイネオス・ヘルス —London
- Bachelor's degree
- Contracts
- Communication skills
Clinical Data & Device Specialist
SAVA —London
- Maths
Quick apply
Clinical Research Project Manager (Part-Time, Maternity Cover)
Mitra Bio —London
- Part-time
- Travel
Trials Manager - Clinical AI Research
Heidi —London
- Full-time
- Project management
- AI
Clinical Evaluation Specialist
Scarlet —London
- £75,000 - £90,000 a year
- Full-time
- Nursing
- Sales
- Patient care
AI Clinical Product Researcher
Odin Vision —London
- £35,000 - £45,000 a year
- Full-time
- Hybrid work
- Engineering
- Bachelor's degree
- Travel
GCP Compliance Manager - Clinical Programs & Trials
Novartis —London
- Full-time
- Hybrid work
- Engineering
- Communication skills
13d
Non-Clinical Assessor - £75,585 - £84,840 p.a. + benefits
Medicines and Healthcare Products Regulatory Agency —London
- £75,585 - £84,840 a year
- Full-time
- Presentation skills
- Travel
- In-person
- Annual leave
- Sick pay
7d
Imaging R&D Specialist
Guy's and St Thomas' NHS Foundation Trust —London
- £66,582 - £77,368 a year
- Full-time
- Travel
- Data entry
- Leadership
9h
Single Sponsor Clinical Trial Manager I (Late Phase) French speaking - Hybrid in London
Syneos - Clinical and Corporate - Prod —London
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Presentation skills
7d
Quality Assurance Project Manager - GCP (with GMP awareness)
Ellipses Pharma —London
- Project management
- Travel
- Communication skills
5d
Principal Clinical Research Specialist
Medtronic —Watford
- £64,800 - £97,200 a year
- Full-time
- Travel
- Organisational skills
- Communication skills
LTO Regulatory Partner
Roche —Welwyn
- Bachelor's degree
- Mentoring
Clinical Evaluation Specialist - Radiology
Scarlet —London
- £75,000 - £90,000 a year
- Full-time
- Nursing
- Sales
- Patient care

I want to receive the latest job alerts for clinical trial regulatory in london, eng

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical trial regulatory jobs near london, eng

Clinical Trial Manager jobs in London

Clinical Research Assistant jobs in West London

Clinical Research Specialist jobs in London

Clinical Research Coordinator jobs in London

Quality Assurance Manager jobs in London

Data Specialist jobs in London

Clinical Research Specialist jobs in Watford

Clinical Research Associate jobs in London

Clinical Research Manager jobs in London

Clinical Trial Manager jobs in University Of York

Hospitality Manager jobs in Manchester

Facilities Manager jobs in Bristol

Clinical Trial Manager jobs in Edinburgh

Clinical Trial Manager jobs in Newcastle Upon Tyne

Retail Store Manager jobs in Glasgow

Clinical Trial Manager jobs in Derby

Clinical Trial Manager jobs in Leeds

Clinical Trial Manager jobs in Manchester

Clinical Research jobs in Remote

Senior Clinical Trial Manager jobs in London

Clinical Research Coordinator

SAVA -
London

Quick apply

Job details

1 hour ago

Qualifications

Clinical research
Communication skills
FDA regulations

Full job description

About SAVA

All the health information we need is within us. Just below the skin. SAVA is redefining the way people interact with their health by developing the most advanced biosensing technology science has to offer, capable of accessing bodily information in a painless, real-time and affordable way.

The Role

The Clinical Research Coordinator supports the delivery of our clinical and performance studies. This is a high-ownership, hands-on role where the Clinical Research Coordinator helps make the wheels of execution turn smoothly. From early-stage testing to pivotal clinical trials, the Clinical Research Coordinator is the force that makes things happen by managing study logistics, participant workflows and data integrity from site setup through to study completion.

The Clinical Research Coordinator works closely with our Clinical Affairs Lead and cross-functional teams at the front line of our studies, coordinating directly with participants, managing devices at the site level and ensuring seamless execution of study protocols. The Clinical Research Coordinator helps build the foundation of our Clinical Operations function while gaining exposure to regulatory processes, data quality, site relationships, and real-world testing. The pace is fast, the problems are complex, and the impact is real.

If you want to directly shape how a novel medical device is tested, validated and ultimately reaches patients, keep reading.

What You’ll Do

Study Operations & Execution:

Own the day-to-day running of studies from startup through site close-out, keeping all moving parts aligned and on schedule
Coordinate study logistics including ethics approvals, regulatory document tracking, and submissions to ensure nothing gets stuck

Device & Supply Management:

Manage investigational device shipments, inventory, and accountability at the site level to ensure full traceability and compliance
Coordinate vendors and supplies with precision
Track device serial numbers, usage, and accountability records to support regulatory compliance

Data Quality & Documentation:

Support data collection and entry into study databases, ensuring accuracy and completeness at every step
Maintain organised, audit-ready documentation across study files, CRFs, and regulatory submissions
Flag data quality issues, protocol deviations, and safety concerns to the Clinical Affairs team immediately

Process Building & Support:

Identify gaps in study workflows and build tools, trackers, and processes that keep operations lean, fast, and compliant
Contribute to SOP development, CRF preparation, and staff training sessions as needed

Compliance & Quality:

Maintain compliance with SAVA's ISO 13485 Quality Management System, policies, and work instructions
Follow all Health and Safety policies and complete required training within timelines

What We’re Looking For

1+ years of experience in clinical research, preferably in medical devices or diagnostics.
Experience working in early-stage or rapidly scaling companies
A background in science, engineering or regulatory affairs
Familiarity with FDA regulations and experience running trials in the US, EU or UK
Strong working knowledge of GCP, ISO 14155 and ethics/regulatory submission processes
Highly organised and detailed-oriented with a proactive mindset
Comfortable with digital tools and trial management systems; quick to learn new platforms
Strong communication and collaboration skills and an ability to thrive in early-stage, fast-moving environments

Bonus Points For

Experience with medical device clinical studies, particularly in sensor or wearable technology, diabetes trials, or CGM.
Experience working in regulated environments, medical devices preferred

Why Sava

This is a high-ownership, high-responsibility role in a company that is building something complex, meaningful, and fast. The expectations are high, the learning curve is steep, and the work is often messy - but the impact is real.

We donʼt have room for egos or passengers. What we do have is a team of thoughtful, driven, and mission-aligned people who are committed to building something better and doing it with urgency and integrity.

Quick apply

Refine Your Search

clinical trial regulatory jobs in london, eng

Clinical Research Coordinator

Clinical Trial Associate Manager

Clinical Research Assistant

Clinical Research Associate, South East England

Clinical Trials Manager

Senior Clinical Trial Administrator

Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)

Clinical Data & Device Specialist

Clinical Research Project Manager (Part-Time, Maternity Cover)

Trials Manager - Clinical AI Research

Clinical Evaluation Specialist

AI Clinical Product Researcher

GCP Compliance Manager - Clinical Programs & Trials

Non-Clinical Assessor - £75,585 - £84,840 p.a. + benefits

Imaging R&D Specialist

Single Sponsor Clinical Trial Manager I (Late Phase) French speaking - Hybrid in London

Quality Assurance Project Manager - GCP (with GMP awareness)

Principal Clinical Research Specialist

LTO Regulatory Partner

Clinical Evaluation Specialist - Radiology

I want to receive the latest job alerts for clinical trial regulatory in london, eng

Related Searches

Explore jobs in more locations

About SAVA

The Role

What You’ll Do

What We’re Looking For

Bonus Points For

Why Sava

Jobseeker tools

Employer Tools

Browse

Stay Connected