Clinical Research Coordinator - #1780727

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

SAVA is hiring a Clinical Research Coordinator to support the delivery of our clinical and performance studies. This is a high-ownership, hands-on role where you will help make the wheels of execution turn smoothly. From early-stage testing to pivotal clinical trials, you will be the force that makes things happen.

This isn’t a passive coordination role - you’ll be in the trenches, working closely with our Senior Clinical Research Manager and cross-functional teams. You will help 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.

What You’ll Do

• Own the day-to-day running of studies: from study start-up to site close-out, you’ll keep everything moving.
• Chase down ethics approvals, track regulatory documents, and make sure submissions don’t get stuck.
• Be the go-to for sites - solving problems, escalating as needed, and keeping everything on track.
• Monitor performance, flag issues early, and follow up relentlessly until they’re fixed.
• Coordinate vendors and supplies meticulously - you will always know what is needed, where it is needed and who needs it by when
• Build the tools and trackers that keep us lean, fast, and compliant.
• Jump in where needed to help write SOPs, prep materials, and support CRF training sessions.
• Get the right information to the right people, at the right time - no ambiguity - trusted and simple communication.
  
  

What We’re Looking For

• 1+ years of experience in clinical research, preferably in medical devices or diagnostics.
• Strong knowledge of GCP, ISO 14155, and ethics/regulatory submission processes in the UK.
• Highly organised, detail-oriented, and proactive - you spot issues before they become problems.
• Seeks satisfaction by completing tasks and reaching milestones.
• Strong communication and collaboration skills; you're comfortable working across teams and with sites.
• Confident using digital tools and trial management systems - and quick to learn new ones.
  
  

Bonus Points For

• Experience working in early-stage or rapidly scaling companies.
• Familiarity with FDA regulations and running trials in the US - or anywhere outside of the UK.
• A background in science, engineering, or regulatory affairs.
  
  

Why SAVA?

This is a high-ownership, high-responsibility role in a company that’s 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 don’t 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.