Clinical research coordinator Work, Jobs in Chesham, Bkm (with Salaries)

Clinical Research Coordinator
SAVA —London
- Communication skills
Quick apply
Clinical Registry Coordinator
ICON Plc —Reading
- Full-time
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
- Employee assistance programme
1d
Part Time Clinical Data Coordinator
HCA Healthcare UK —London
- Up to £13,600 a year
- Part-time
- Employee discount
17h
Trial Coordinator
ICR —London
- £31,445 - £33,600 a year
- Travel
- IT
11d
MBBS Assessment Coordinator
University College London —London
- £43,981 - £52,586 a year
- Full-time
- No degree
- Annual leave
- Employee assistance programme
1d
Clinical Data Coordinator
HCA Healthcare UK —London
- Up to £34,000 a year
- Full-time
- Employee discount
17h
Clinical Registry Coordinator - UK Based
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
1d
Linguistic Validation & eCOA Team Lead
IQVIA —Reading
- Full-time
- Hybrid work
- Customer service
- Microsoft Office
- Bachelor's degree
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Administration Coordinator
University College London Hospitals NHS Foundation Trust —London
- £34,186 - £37,389 a year
- Part-time
- Customer service
- Communication skills
4h
Senior Research Assistant Practitioner
The Royal Marsden NHS Foundation Trust —Chelsea
- £38,488 - £46,852 a year
- Full-time
- Rehabilitation centre
- Organisational skills
- Leadership
10h
Technical Product Manager - (Clinical Integrations) - UK
Heidi —London
- Full-time
- Hybrid work
- Master's degree
- Bachelor's degree
- SharePoint
Activity Co-ordinator
Central and North West London NHS Foundation Trust —London
- £34,186 - £37,389 a year
- Part-time
- Care plans
- Communication skills
- School
2d
Senior Site Activation Coordinator
IQVIA —Reading
- Full-time
- Hybrid work
11d
Senior Trials Manager
University College London —London
- £54,931 - £64,644 a year
- Full-time
- Hybrid work
- Bachelor's degree
15h
Gynaecology Service Manager
London North West University Healthcare NHS Trust —London
- £55,524 - £62,652 a year
- Full-time
- Analysis skills
- Hospice
- Leadership
3d
Palliative Care Clinical Nurse Specialist
Royal Free London NHS Foundation Trust —London
- £55,524 - £62,652 a year
- Full-time
- IT
- Communication skills
3d
Senior Registered Veterinary Nurse - HDU & Wards
IVC —High Wycombe
- Up to £37,500 a year
- Weekend availability
- Leadership
- Nursing
- Annual leave
- Employee discount
Band 7 Clinical Psychologist - BCYP
Royal Free London NHS Foundation Trust —London
- £55,524 - £62,652 a year
- Full-time
- Care plans
9d
Psychologist
Central and North West London NHS Foundation Trust —London
- £58,133 - £65,261 a year
- Full-time
- Care plans
7d

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clinical research coordinator jobs near chesham, bkm

Clinical Research Coordinator

SAVA -
London

Quick apply

Job details

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 coordinator jobs in chesham, bkm

Clinical Research Coordinator

Clinical Registry Coordinator

Part Time Clinical Data Coordinator

Trial Coordinator

MBBS Assessment Coordinator

Clinical Data Coordinator

Clinical Registry Coordinator - UK Based

Linguistic Validation & eCOA Team Lead

Clinical Trials Manager

Administration Coordinator

Senior Research Assistant Practitioner

Technical Product Manager - (Clinical Integrations) - UK

Activity Co-ordinator

Senior Site Activation Coordinator

Senior Trials Manager

Gynaecology Service Manager

Palliative Care Clinical Nurse Specialist

Senior Registered Veterinary Nurse - HDU & Wards

Band 7 Clinical Psychologist - BCYP

Psychologist

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About SAVA

The Role

What You’ll Do

What We’re Looking For

Bonus Points For

Why Sava

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