Clinical Trial Associate

TFS HealthScience; London; On-site; GBP 30,000 - 45,000; Full time

Job summary

TFS HealthScience is seeking a Clinical Trial Associate for an on-site role in London. The position offers an opportunity to support clinical projects, maintain compliance, and develop your career in a collaborative environment. Ideal candidates will have experience in clinical research and strong organizational skills.

Qualifications

• Some previous experience as a CTA or in a clinical research support role.
• Understanding of clinical research processes and GCP guidelines.
• Ability to work on-site in the UK.

Responsibilities

• Support the clinical project team in the preparation and tracking of study documents.
• Maintain Trial Master File (TMF) in compliance with ICH-GCP.
• Track and manage study-related information including site details.

Skills

Organizational skills

Attention to detail

Communication

Interpersonal skills

Proficiency with Microsoft Office

Job description

TFS HealthScience is a global, mid-sized Contract Research Organization (CRO) dedicated to supporting biotechnology and pharmaceutical companies throughout their clinical development journey. We provide full-service capabilities, resourcing, and Functional Service Provider (FSP) solutions to help bring innovative therapies to patients worldwide.

We are currently seeking a Clinical Trial Associate(CTA) for an on-site role in the United Kingdom. This is an excellent opportunity for someone with some prior experience in clinical trial administration who is looking to continue developing their career in a supportive and collaborative environment.

Key Responsibilities

Support the clinical project team in the preparation, distribution, and tracking of study documents

Maintain Trial Master File (TMF) in compliance with ICH-GCP and sponsor requirements

Assist with the coordination of ethics submissions and study start-up activities

Track and manage study-related information including site and investigator details, training records, and study documentation

Support meeting coordination, minutes, and follow-up tasks

Communicate effectively with internal teams, clinical sites, and sponsors

Qualifications

Some previous experience as a CTA or in a clinical research support role (CRO, pharmaceutical company, or academic research environment)

Understanding of clinical research processes and GCP guidelines

Strong organizational skills and attention to detail

Good communication and interpersonal skills

Proficiency with Microsoft Office and basic document management systems

Ability to work on-site in the UK (location will be confirmed during the process)

A Bit More About Us

Founded over 27 years ago in Lund, Sweden, TFS HealthScience is a full-service, global CRO with more than 800 professionals delivering tailored clinical research services in over 40 countries. We support clinical development across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

Our values—Trust, Quality, Passion, Flexibility, and Sustainability—shape our culture and drive our mission to improve patient lives through clinical research.