Clinical Trial Assistant

Indo Search

Swansea

On-site

GBP 24,000 - 32,000

Full time

14 days+
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Job summary

A leading MedTech company in Swansea is seeking a Clinical Trial Assistant to support clinical operations for trials in a dynamic environment. The ideal candidate has GCP training and at least 1 year of experience. This role involves managing participant schedules and ensuring data accuracy. Opportunities for growth and hands-on training are provided, making it perfect for those looking to build a clinical career in medical devices.

Qualifications

  • At least 1 year of experience supporting clinical trials or a similar regulated health/research setting.
  • Must have completed Good Clinical Practice (GCP) training.
  • Strong organizational skills and meticulous attention to detail.
  • Confidence in communicating with participants and managing sensitive information.
  • Flexible approach to working hours (some evenings required).

Responsibilities

  • Support the clinical team through all phases of study delivery.
  • Coordinate participant schedules and manage informed consent.
  • Administer investigational treatments and capture imaging data.
  • Conduct skin measurements and monitor patient safety.
  • Ensure accurate data entry into trial systems.
  • Maintain audit-ready documentation and manage clinical supplies.
  • Help maintain audit-ready documentation and manage clinical supplies.

Skills

GCP training
Organizational skills
Attention to detail
Communication skills
Team-oriented attitude

Job description

Overview

Clinical Trial Assistant – Medical Devices

Please read before applying – essential requirements.

To be considered, you must:

  • Already have the right to work in the UK (no sponsorship available).
  • Be based within daily commuting distance of Swansea, or able to relocate.
  • Have completed Good Clinical Practice (GCP) training.
  • Have at least 1 year of experience working in a clinical research or trial-related role.

Applications that do not clearly demonstrate these will not be progressed due to expected high volumes.

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)

Reports to: CTA Manager

Why now?

With major clinical trials underway and investment in new product development, this team is growing fast. 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.

Seniority level
  • Entry level
Employment type
  • Full-time
Job function
  • Research and Science
Industries
  • Medical Equipment Manufacturing
  • Pharmaceutical Manufacturing
  • Biotechnology Research
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