Clinical affairs Work, Jobs in London (with Salaries)

Clinical Research Coordinator
SAVA —London
- Communication skills
Quick apply
16h
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
8d
Medical Writer, MedComms & Publications
Envision Pharma Group —London
- Full-time
- Remote
- Microsoft Office
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Spanish
- Microsoft Excel
Quick apply
Scientific Editor
WebMD —London
- Full-time
- Microsoft Office
- Bachelor's degree
- Organisational skills
Quick apply
Content Writer - Pharmacovigilance
RxLogix Corporation —London
- Full-time
- Hybrid work
- Bachelor's degree
- Medical terminology
Quick apply
Medical Affairs Partner
Roche —Welwyn
- Bachelor's degree
- Mentoring
- Communication skills
5d
Clinical Research Scientist - Medical Affairs
Skin Analytics Ltd —London
- Full-time
- Google Suite
- Doctoral degree
- Data analysis skills
- Annual leave
Quick apply
1d
Medical Strategist
MEDiSTRAVA —London
- Remote
- Doctoral degree
- Master's degree
- Project management
Clinical Research Project Manager (Part-Time, Maternity Cover)
Mitra Bio —London
- Part-time
- Travel
Quality Assurance & Regulatory Affairs Specialist
Pangaea Data —London
- Communication skills
- Flexible schedule
- Life insurance
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Clinical Home Manager at Wellesley Road
Shaw Healthcare —London
- £70,000 - £75,000 a year
- Leadership
- Annual leave
- Referral programme
1d
Medical Science Liaison (UK)
Pharmanovia —London
- Hybrid work
- Doctoral degree
- English
- Travel
Medical Writer II - Publications
サイネオス・ヘルス —London
- £70,100 - £145,000 a year
- English
- Travel
- Contracts
- Employee stock purchase plan
- Annual leave
Regulatory Affairs Associate/Manager
Transpire BIO Inc. —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Senior Manager Medical Information
Vertex Pharmaceuticals —Paddington
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- In-person
11d
Medical Science Liaison
Syneos Health Commercial Solutions —London
- Doctoral degree
- Travel
Clinical Data & Device Specialist
SAVA —London
- Maths
Quick apply
Scientific Affairs Manager, UK - London
Rhythm Pharmaceuticals —London
- Full-time
- Doctoral degree
- Presentation skills
- Communication skills

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clinical affairs jobs near london

Clinical Research Coordinator

SAVA -
London

Quick apply

Job details

16 hours 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 affairs jobs in london

Clinical Research Coordinator

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

Medical Writer, MedComms & Publications

Medical Information Specialist - US Hours

Scientific Editor

Content Writer - Pharmacovigilance

Medical Affairs Partner

Clinical Research Scientist - Medical Affairs

Medical Strategist

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

Quality Assurance & Regulatory Affairs Specialist

Clinical Trials Manager

Clinical Home Manager at Wellesley Road

Medical Science Liaison (UK)

Medical Writer II - Publications

Regulatory Affairs Associate/Manager

Senior Manager Medical Information

Medical Science Liaison

Clinical Data & Device Specialist

Scientific Affairs Manager, UK - London

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