Clinical research operations Work, Jobs in London, Eng (with Salaries)

Clinical Research Coordinator
SAVA —London
- Communication skills
Quick apply
4d
Research Assistant - Bank
hVIVO Services Limited —London
- Weekend availability
- Laboratory experience
- Communication skills
3d
Clinical Research Project Manager (Part-Time, Maternity Cover)
Mitra Bio —London
- Part-time
- Travel
Diagnostic Archive Research Tissue Bank Operations Manager
The Royal Marsden NHS Foundation Trust —Chelsea
- £58,133 - £65,261 a year
- Full-time
- Laboratory experience
- Communication skills
8d
Senior Research Technician / Co-ordinator
Imperial College London —Charing Cross
- £46,614 - £56,345 a year
- Full-time
- Laboratory experience
- Organisational skills
- Annual leave
10d
Clinical Trials Manager
Imperial College London —London
- £46,614 - £56,345 a year
- Full-time
10d
Trials Manager - Clinical AI Research
Heidi —London
- Full-time
- Project management
- AI
Study Manager, Clinical Operations
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Project management
Quick apply
Clinical Evaluation Specialist
Scarlet —London
- £75,000 - £90,000 a year
- Full-time
- Nursing
- Sales
- Patient care
Project Management Team Lead – Clinical Trials (f/m/d)
Clariness GmbH —London
- Full-time
- English
- Project management
- Mentoring
- Flexible schedule
Quick apply
9d
Clinical Operations Lead Early Phase Oncology
Excelya —London
- Full-time
- Hybrid work
- English
- Master's degree
Quick apply
Clinical Operations & Enablement Lead
Nucs AI —London
- Full-time
- Hybrid work
- Master's degree
- Presentation skills
- Bachelor's degree
Quick apply
Technical Program Manager, Human Research Lab Operations
Google —London
- Bachelor's degree
GCP Compliance Manager - Clinical Programs & Trials
Novartis —London
- Full-time
- Hybrid work
- Engineering
- Communication skills
Research Technician - Part-time - 0.8 FTE
University College London —London
- £36,433 - £41,833 a year
- Part-time
- Doctoral degree
- Master's degree
- University
- Annual leave
- Employee assistance programme
Clinical Project Manager II
Perceptive —London
- Full-time
- PMP
- No experience needed
- English
Clinical Trial Associate Manager
Galderma —London
- Hybrid work
- Project management
- Bachelor's degree
- Leadership
Principal Clinical Research Specialist
Medtronic —Watford
- £64,800 - £97,200 a year
- Full-time
- Travel
- Organisational skills
- Communication skills
AI Agent Operations Specialist (FTE 60%)
Delfa AI —London
- APIs
- AI
Quick apply
People Operations Specialist
Pangaea Data —London
- Human resources
- Contracts
- Communication skills
- Flexible schedule
- Life insurance

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clinical research operations jobs near london, eng

Clinical Research Coordinator

SAVA -
London

Quick apply

Job details

4 days 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 research operations jobs in london, eng

Clinical Research Coordinator

Research Assistant - Bank

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

Diagnostic Archive Research Tissue Bank Operations Manager

Senior Research Technician / Co-ordinator

Clinical Trials Manager

Trials Manager - Clinical AI Research

Study Manager, Clinical Operations

Clinical Evaluation Specialist

Project Management Team Lead – Clinical Trials (f/m/d)

Clinical Operations Lead Early Phase Oncology

Clinical Operations & Enablement Lead

Technical Program Manager, Human Research Lab Operations

GCP Compliance Manager - Clinical Programs & Trials

Research Technician - Part-time - 0.8 FTE

Clinical Project Manager II

Clinical Trial Associate Manager

Principal Clinical Research Specialist

AI Agent Operations Specialist (FTE 60%)

People Operations Specialist

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