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For Companies At a Glance
- Tasks: Monitor clinical imaging data for trials, ensuring compliance and quality.
- Company: Join a pioneering tech company revolutionising clinical trial monitoring with advanced digital solutions.
- Benefits: Enjoy flexible freelance hours, competitive pay, and prompt payments.
- Why this job: Be at the forefront of innovative imaging studies in a supportive, tech-driven environment.
- Qualifications: Must have CRA experience in the UK and knowledge of clinical imaging standards.
- Other info: Remote work options available, with travel across the UK for onsite visits.
The predicted salary is between 36000 - 60000 £ per year.
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.
Freelance Clinical Research Associate employer: Pivot Search
Contact Detail:
Pivot Search Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Freelance Clinical Research Associate
✨Tip Number 1
Network with professionals in the clinical imaging field. Attend relevant conferences or webinars to meet potential colleagues and learn about the latest trends in imaging technology, which can give you an edge during interviews.
✨Tip Number 2
Familiarise yourself with the specific imaging modalities mentioned in the job description, such as MRI, CT, and PET. Being able to discuss these technologies confidently will demonstrate your expertise and commitment to the role.
✨Tip Number 3
Showcase your experience with digital platforms and remote monitoring tools. Be prepared to discuss how you've successfully used technology in previous roles to enhance data quality and compliance.
✨Tip Number 4
Prepare for questions about ICH-GCP and UK regulations. Brush up on these guidelines to ensure you can articulate your understanding and how it applies to imaging data management in clinical trials.
We think you need these skills to ace Freelance Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience as a Clinical Research Associate, particularly in imaging and clinical trials. Emphasise your familiarity with ICH-GCP and UK regulations, as well as any specific imaging modalities you have worked with.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of imaging data management. Mention specific experiences that demonstrate your ability to conduct monitoring visits and liaise effectively with study teams and imaging sites.
Highlight Technical Skills: Since the role focuses heavily on tech-enabled monitoring, be sure to mention your proficiency with digital platforms and remote monitoring technologies. Provide examples of how you've successfully used these tools in previous roles.
Showcase Communication Abilities: In your application, illustrate your excellent communication skills by providing examples of how you've collaborated with radiologists, vendors, and study teams. This will help demonstrate your ability to work effectively in a team-oriented environment.
How to prepare for a job interview at Pivot Search
✨Showcase Your Clinical Imaging Knowledge
Make sure to highlight your experience with clinical imaging during the interview. Be prepared to discuss specific imaging modalities you've worked with, such as MRI or CT, and how you've ensured data quality in previous roles.
✨Demonstrate Familiarity with Regulations
Brush up on ICH-GCP and UK regulations relevant to clinical trials. Being able to articulate your understanding of these guidelines will show that you are well-prepared and knowledgeable about compliance in clinical research.
✨Emphasise Your Tech Savviness
Since this role focuses heavily on digital platforms for monitoring, be ready to discuss your experience with remote monitoring technologies. Share examples of how you've effectively used digital tools in past projects to enhance data capture and oversight.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think of examples where you had to resolve issues related to imaging data or liaise with study teams, and be ready to explain your thought process and actions taken.