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- Tasks: Manage clinical studies from start to finish, ensuring everything runs smoothly.
- Company: SAVA is revolutionising health interaction with cutting-edge biosensing technology.
- Benefits: Enjoy a high-responsibility role with opportunities for growth and learning.
- Why this job: Be part of a mission-driven team making a real impact in healthcare.
- Qualifications: 1+ years in clinical research; strong organisational and communication skills required.
- Other info: Fast-paced environment with a focus on collaboration and problem-solving.
The predicted salary is between 30000 - 42000 £ per year.
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 Associate 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.
Clinical Research Coordinator employer: SAVA
Contact Detail:
SAVA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Coordinator
✨Tip Number 1
Familiarise yourself with the latest trends in clinical research, especially in medical devices and diagnostics. This knowledge will not only help you during interviews but also demonstrate your genuine interest in the field.
✨Tip Number 2
Network with professionals already working in clinical research or at SAVA. Attend industry events or join relevant online forums to connect with others who can provide insights or even refer you for the position.
✨Tip Number 3
Prepare to discuss specific examples from your past experience that showcase your organisational skills and problem-solving abilities. Be ready to explain how you've successfully managed projects or resolved issues in a fast-paced environment.
✨Tip Number 4
Showcase your familiarity with digital tools and trial management systems by mentioning any relevant software you've used. If you haven't used specific tools mentioned in the job description, express your eagerness to learn them quickly.
We think you need these skills to ace Clinical Research Coordinator
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research, particularly in medical devices or diagnostics. Emphasise your knowledge of GCP, ISO 14155, and any regulatory submission processes you've encountered.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your proactive approach to problem-solving. Mention specific examples from your past experiences that demonstrate your organisational skills and ability to work across teams.
Highlight Relevant Skills: In your application, clearly outline your strong communication and collaboration skills. Provide examples of how you've successfully coordinated projects or resolved issues in previous roles, especially in fast-paced environments.
Show Enthusiasm for the Role: Convey your excitement about the opportunity at SAVA. Discuss why you are drawn to their mission of redefining health interaction and how your values align with their commitment to urgency and integrity.
How to prepare for a job interview at SAVA
✨Show Your Passion for Clinical Research
Make sure to express your enthusiasm for clinical research and the impact it has on health technology. Share specific examples of how your previous experiences have prepared you for this role, especially in medical devices or diagnostics.
✨Demonstrate Organisational Skills
Since the role requires meticulous coordination, be ready to discuss how you manage multiple tasks and keep everything on track. Prepare examples that showcase your ability to stay organised and proactive in problem-solving.
✨Familiarise Yourself with Relevant Regulations
Brush up on GCP, ISO 14155, and UK regulatory submission processes before the interview. Being able to discuss these topics confidently will show that you understand the complexities of the role and are prepared to navigate them.
✨Highlight Communication Skills
Effective communication is key in this position. Be prepared to share instances where you successfully collaborated with cross-functional teams or resolved issues with sites. This will demonstrate your ability to convey information clearly and build strong relationships.
