Clinical Trial Coordinator in London
Clinical Trial Coordinator

Clinical Trial Coordinator in London

London Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Coordinate clinical trials and ensure smooth operations while maintaining high ethical standards.
  • Company: Join myota, a pioneering startup transforming gut health with innovative science.
  • Benefits: Autonomy from Day 1, career development, and a free subscription to gut health products.
  • Why this job: Make a real impact on health while working with leading scientists in a dynamic environment.
  • Qualifications: Degree in life sciences and experience in clinical trials or human research studies.
  • Other info: Work in central London with a small, creative team and a friendly office dog.

The predicted salary is between 36000 - 60000 £ per year.

About us

At myota, we’re transforming gut health with cutting-edge science and clinically proven innovation. Founded by world-leading microbiome scientists and seasoned operators, and backed by Europe’s top VCs, myota is pioneering a new era of prebiotic fibre products — clinically effective, patented, and built on groundbreaking research from MIT. With over 50,000 customers and strong adoption among doctors, dietitians and nutritionists, we’re already making a meaningful difference. Our clinical research programme spans partnerships with the NHS and leading universities, placing us at the forefront of evidence-based gut health. You’ll be joining us at a pivotal moment in our growth — a small, high-impact team on a mission to prevent and reverse the 1 billion cases of chronic disease linked to poor gut health. We’re here to extend healthy lifespans, one gut at a time.

About the role

We are looking for a motivated and organised Clinical Trial Coordinator (full-time, 12-month fixed-term) to support the delivery of clinical trials at myota. This role is ideal for someone with prior experience in human research studies who is ready to take on increased responsibility in a dynamic, mission-driven startup. You will play a central role in the day-to-day coordination of our clinical trials, helping to ensure all activities run smoothly and to the highest ethical and regulatory standards. The role offers hands-on experience across multiple aspects of clinical trial delivery. You will be required to be on-site at our London office full-time to deliver clinical trial activities.

Key responsibilities

  • Project coordination: Support the planning and operational delivery of clinical trials, from ethics submission to final data collection
  • Regulatory & ethics: Prepare and maintain documentation for ethics committees and other relevant bodies
  • SOPs & documentation: Maintain study documentation and trial master files in compliance with regulatory standards
  • Site & vendor communication: Liaise with study sites, labs, couriers, and external vendors to support smooth trial operations
  • Participant recruitment & retention: Help coordinate recruitment activities and track participant enrolment and communication
  • Data collection & quality control: Support data entry, monitoring, and verification, ensuring accuracy and completeness
  • Logistics: Manage supplies, sample kits, and shipment schedules, including packaging and coordinating deliveries where required
  • Reporting: Assist with progress updates, summaries, and internal reporting for the project team

What we’re looking for

  • BSc or above (MSc desirable) degree in life sciences, health sciences, nutrition, or a related field
  • Experience coordinating or supporting clinical trials or human research studies (e.g., in NHS, academic, or commercial settings)
  • Working knowledge of Good Clinical Practice (GCP) and research governance
  • Excellent organisational and time management skills
  • Strong attention to detail and ability to follow SOPs and protocols
  • Good written and verbal communication skills
  • Familiarity with data entry systems or EDC platforms

Desirable

  • Experience working in a startup or small team environment
  • GCP certification
  • Familiarity with ethics submissions (e.g., IRAS, REC, HRA)

What you’ll get

  • Autonomy and real responsibility from Day 1: You’ll be owning and driving key projects from the very start, making a direct impact on our growth and giving you the chance to learn and develop lots of new skills.
  • Work directly with the founding team: You’ll collaborate closely with our experienced founders, gaining invaluable insights into the workings of a fast-growing start-up and the wider business landscape.
  • Career development: You’ll be part of a rapidly expanding company with endless opportunities for personal and professional growth.
  • Become a gut health pro: Work alongside leading PhD scientists, deepening your knowledge of the microbiome and becoming an expert in gut health.
  • Dynamic & creative work environment: Join a small, innovative team that values creativity and new ideas, and where your contributions will truly make a difference.
  • Central London location: Work from our office (and with part-time office dog Winston) in the heart of a vibrant start-up community.
  • Top-notch equipment: All the tools you need to succeed, including a laptop, monitor, and any other equipment required.
  • Free myota subscription: Stay healthy with a complimentary subscription to our innovative gut health products.

Clinical Trial Coordinator in London employer: myota

At myota, we pride ourselves on being an exceptional employer, offering a dynamic and creative work environment in the heart of Central London. As a Clinical Trial Coordinator, you will have the opportunity to take on real responsibility from day one, working closely with our founding team and leading scientists to make a meaningful impact on gut health. With a strong focus on personal and professional growth, we provide endless opportunities for development, alongside top-notch equipment and a complimentary subscription to our innovative products.
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Contact Detail:

myota Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Trial Coordinator in London

✨Tip Number 1

Network like a pro! Reach out to people in the industry, attend relevant events, and connect with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.

✨Tip Number 2

Prepare for interviews by researching myota and understanding their mission. Be ready to discuss how your skills align with their goals in gut health. Show them you’re not just another candidate, but someone who genuinely cares about their mission.

✨Tip Number 3

Practice your responses to common interview questions, especially those related to clinical trials and project coordination. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your experience effectively.

✨Tip Number 4

Don’t forget to follow up after your interview! A simple thank-you email can go a long way in showing your enthusiasm for the role. Plus, it keeps you fresh in their minds as they make their decision.

We think you need these skills to ace Clinical Trial Coordinator in London

Project Coordination
Regulatory Compliance
Good Clinical Practice (GCP)
Organisational Skills
Time Management
Attention to Detail
Written Communication Skills
Verbal Communication Skills
Data Entry Systems
Ethics Submissions
Participant Recruitment
Quality Control
Logistics Management
Collaboration Skills

Some tips for your application 🫡

Show Your Passion for Gut Health: When writing your application, let your enthusiasm for gut health shine through! We want to see how your background and interests align with our mission at myota. Share any relevant experiences that highlight your commitment to improving health through innovative science.

Tailor Your CV and Cover Letter: Make sure to customise your CV and cover letter for the Clinical Trial Coordinator role. Highlight your experience in clinical trials and any specific skills that match the job description. This shows us you’ve done your homework and are genuinely interested in joining our team.

Be Clear and Concise: Keep your application clear and to the point. Use straightforward language and avoid jargon unless it’s relevant. We appreciate a well-structured application that makes it easy for us to see your qualifications and fit for the role.

Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it gives you a chance to explore more about myota and what we stand for.

How to prepare for a job interview at myota

✨Know Your Stuff

Make sure you brush up on the latest in gut health and clinical trials. Familiarise yourself with myota's products and their impact on gut health. This will show your genuine interest and help you connect your experience to their mission.

✨Showcase Your Organisational Skills

As a Clinical Trial Coordinator, organisation is key. Prepare examples of how you've successfully managed projects or trials in the past. Be ready to discuss specific tools or methods you used to keep everything on track.

✨Communicate Clearly

Strong communication skills are essential for this role. Practice articulating your thoughts clearly and concisely. You might be asked about how you would handle communication with study sites or participants, so have some scenarios in mind.

✨Ask Insightful Questions

Prepare thoughtful questions about myota’s clinical research programme and their approach to gut health. This not only shows your enthusiasm but also helps you gauge if the company culture aligns with your values and career goals.

Clinical Trial Coordinator in London
myota
Location: London

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