Freelance Clinical Research Associate

Freelance Clinical Research Associate (CRA) – UK (Imaging Focus)

About My Client

My client is a pioneering clinical trial technology company specialising in imaging-based trial monitoring and data integrity solutions. They leverage advanced digital platforms to provide seamless, real-time oversight of clinical imaging data, ensuring compliance, quality, and patient safety across global studies.

The Role

They are seeking experienced Freelance Clinical Research Associates (CRAs) based in the UK with a strong understanding of clinical imaging to support the monitoring of their innovative imaging-centric clinical trials. You will play a crucial role in ensuring accurate, compliant, and timely capture and review of imaging data within clinical studies.

Key Responsibilities

• Conduct remote and onsite monitoring visits focused on imaging data quality and protocol adherence
• Review imaging data, related source documentation, and patient records to verify accuracy and compliance with study protocols and regulatory guidelines
• Liaise with imaging sites, radiologists, and study teams to resolve queries and ensure high-quality image acquisition and transfer
• Support site initiation, routine monitoring, and close-out visits with an imaging focus
• Escalate any deviations or issues related to imaging processes in a timely manner
• Maintain thorough monitoring documentation and provide regular status updates to study teams
• Support the adoption and effective use of digital tools for imaging data capture and remote monitoring

What You’ll Need

• Proven CRA experience in the UK with exposure to clinical imaging, radiology, or imaging data management within clinical trials
• Strong knowledge of ICH-GCP, UK regulations, and imaging standards applicable to clinical research
• Familiarity with imaging modalities (e.g., MRI, CT, PET) and experience reviewing imaging-related documentation
• Comfortable using digital platforms and remote monitoring technologies — this role focuses heavily on tech-enabled monitoring
• Excellent communication skills and ability to work collaboratively with imaging sites, vendors, and study teams
• Ability to manage your workload independently and travel across the UK for onsite visits as required
• Relevant scientific or clinical qualifications (Life Sciences degree, Radiography, or equivalent clinical research experience)

Why Work With My Client?

• Flexible freelance contract allowing you to manage your schedule and workload
• Competitive day rates with prompt payment terms
• Opportunity to work at the forefront of digital imaging trial monitoring on exciting, cutting-edge studies
• Supportive, innovation-driven culture committed to quality and transparency