Clinical Trial Assistant
Full-time
Primarily site-based, London
£30,000 to £35,000
Please read carefully before applying.
This is a highly hands-on Clinical Trial Assistant role with direct participant interaction and practical involvement in the day-to-day delivery of clinical studies.
Essential requirements
You must:
• Have full, unrestricted right to work in the UK on a long-term basis
• Not require current or future visa sponsorship
• Not be subject to post-study work visa time restrictions
• Already be based within commuting distance of London, or willing to relocate before starting
• Have some exposure to clinical research, healthcare, or patient-facing clinical environments
• Be comfortable interacting directly with participants and carrying out practical clinical trial procedures
• Have strong communication skills, attention to detail, and confidence working within protocols and regulated processes
Experience with ICH GCP is preferred, but formal certification is not essential.
Applications requiring current or future sponsorship support cannot be considered.
The opportunity
This is an opportunity to join a growing clinical team within an established company developing non-invasive treatment technologies used internationally.
The company runs a significant amount of its clinical work internally, and the CTA team plays a central role in the day-to-day delivery of studies.
You will work directly with participants throughout the clinical trial process, supporting treatments, imaging, measurements, photography, consent procedures and ongoing participant interaction.
The environment would suit someone who enjoys practical involvement, working closely with people, and being part of a collaborative clinical team.
What you will be doing
• Supporting clinical studies from start-up through to close out
• Coordinating participant visits and day-to-day trial activities
• Managing informed consent and participant documentation
• Carrying out protocol-driven procedures and assessments
• Supporting non-invasive investigational treatments
• Operating specialist imaging and photography equipment
• Recording study data and maintaining accurate study records
• Supporting compliance with ICH GCP, ISO 14155 and internal SOPs
• Working closely with participants to ensure a positive clinical trial experience
Who this role could suit
This role could suit someone with experience or exposure within:
• Clinical trials
• Nursing or healthcare support
• Patient-facing healthcare environments
• Clinical research delivery
• Medical devices, pharma or aesthetics
• Allied healthcare professions
• Life sciences graduates with practical healthcare experience
Working pattern
Primarily site-based in London.
Some hybrid flexibility is available once fully trained and established within the role.
Why apply
This is an opportunity to gain genuine hands-on clinical trial experience with far greater day-to-day involvement in study delivery than many traditional CTA positions.
You will become directly involved in participant interaction, protocol-driven procedures and clinical trial operations within a supportive and experienced team environment.
For the right person, this offers strong long-term development within clinical research.
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