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- Tasks: Support clinical trials from start to finish, engaging with patients and managing data.
- Company: Join a leading MedTech company revolutionising beauty technology with innovative, non-invasive devices.
- Benefits: Enjoy structured onboarding, growth opportunities, and hands-on experience in a dynamic team.
- Why this job: Gain real-world clinical research experience while making a difference in patient care.
- Qualifications: Must have 1 year of clinical trial experience and GCP training.
- Other info: Positions available in Swansea or London, with competitive salaries based on location.
The predicted salary is between 26000 - 35000 £ per year.
Job Description
Clinical Trial Assistant – Medical Devices
Full-time, site-based – Swansea (£26,000–£28,000) or London (£30,000–£35,000)
Must have prior experience in a clinical research setting and GCP training
If you’ve ever wanted hands-on clinical trial experience in a regulated, high-performance research setting, this is your chance.
This growing MedTech company is a global leader in light-based beauty technology. Their CE-marked, non-invasive devices are sold in over 50 countries and backed by serious clinical rigour.
Now, they’re expanding their UK clinical team and hiring two Clinical Trial Assistants to help deliver a new wave of studies from their Swansea and London sites.
This isn’t a desk job. You’ll be right in the thick of clinical trial operations, from patient interaction to data management, helping to ensure every trial is delivered to the highest quality.
What you’ll be doing:
- Supporting the clinical team through all phases of study delivery (start-up to close-out)
- Coordinating participant schedules and managing informed consent
- Administering light-based investigational treatments and capturing high-quality imaging data
- Conducting non-invasive skin measurements and monitoring patient safety
- Ensuring complete, accurate and timely data entry into CRFs and trial systems
- Upholding GCP, ISO 14155, and internal SOPs at every step
- Helping maintain audit-ready documentation and managing clinical supplies
What makes this different?
You won’t just be observing from the sidelines, you’ll be trained and trusted to deliver study activities yourself.
From clinical photography to hands-on support with device treatments, this role offers genuine exposure to regulated clinical research within a close-knit team. The company invests in its people, offers a structured onboarding programme, and creates opportunities for growth within the research function.
What you’ll need:
- At least 1 year of experience supporting clinical trials (or similar regulated health/research setting)
- GCP training and a good understanding of trial documentation
- Strong organisational skills and meticulous attention to detail
- Confidence in communicating with participants and managing sensitive information
- A team-oriented, can-do attitude and flexible approach to working hours (some evenings required)
Location: On-site at either Swansea (£26,000–£28,000) or London (£30,000–£35,000)
Reports to: CTA Manager
Why now?
With major clinical trials underway and investment in new product development, this team is growing fast, and these roles are ideal for someone looking to build a long-term clinical career in the medical device space.
If you’re ready to step into a dynamic, regulated clinical environment and help bring effective, high-quality products to patients around the world, apply today.
Clinical Trial Assistant employer: Indo Search
Contact Detail:
Indo Search Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Assistant
✨Tip Number 1
Familiarise yourself with the specific clinical trial processes and regulations, especially GCP and ISO 14155. Understanding these guidelines will not only help you in interviews but also demonstrate your commitment to quality and compliance in clinical research.
✨Tip Number 2
Network with professionals in the clinical research field, particularly those who have experience with medical devices. Attend industry events or join relevant online forums to connect with potential colleagues and learn more about the role and company culture.
✨Tip Number 3
Prepare to discuss your previous experiences in clinical trials during the interview. Be ready to share specific examples of how you've contributed to study delivery, managed participant interactions, or ensured data accuracy, as this will highlight your hands-on experience.
✨Tip Number 4
Showcase your organisational skills by discussing how you manage multiple tasks and maintain attention to detail. This role requires juggling various responsibilities, so demonstrating your ability to stay organised under pressure will make you a strong candidate.
We think you need these skills to ace Clinical Trial Assistant
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical trials and GCP training. Use specific examples that demonstrate your skills in supporting clinical research and managing trial documentation.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the role. Mention why you are interested in working with this MedTech company and how your background aligns with their mission.
Highlight Relevant Skills: In your application, emphasise your organisational skills, attention to detail, and ability to communicate effectively with participants. These are crucial for the Clinical Trial Assistant role and should be clearly articulated.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application reflects your professionalism and attention to detail, which is vital in a regulated environment.
How to prepare for a job interview at Indo Search
✨Showcase Your Clinical Experience
Make sure to highlight your previous experience in clinical research settings. Be prepared to discuss specific trials you've worked on, your role, and how you contributed to their success.
✨Demonstrate GCP Knowledge
Since GCP training is a must for this role, be ready to explain key principles of Good Clinical Practice. You might be asked how you’ve applied these principles in past roles, so have examples at the ready.
✨Emphasise Attention to Detail
This position requires meticulous attention to detail, especially when it comes to data entry and documentation. Prepare to discuss how you ensure accuracy in your work and any systems you use to maintain high standards.
✨Prepare for Patient Interaction Scenarios
As you'll be interacting with participants, think about how you would handle sensitive information and communicate effectively. Consider role-playing potential scenarios to build your confidence before the interview.
