Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Support clinical trials by managing logistics, collecting data, and assisting in procedures.
- Company: Join a pioneering company developing cutting-edge cardiac ablation technologies.
- Benefits: Enjoy international travel opportunities and gain hands-on experience in the medical field.
- Why this job: Be part of innovative clinical research that impacts patient care and advances medical technology.
- Qualifications: 3+ years in clinical trials, knowledge of human anatomy, and proficiency in relevant software.
- Other info: Candidates must have direct experience with medical devices; pharmaceutical experience is not accepted.
The predicted salary is between 36000 - 60000 £ per year.
Job Description
Ready to start a new adventure?
Our client is developing next-generation cardiac ablation technologies and is seeking a Clinical Trial Support Specialist to provide procedural case support, manage device logistics, and collect study data across international sites.
This international role is ideal for a professional with medical device trial experience who is comfortable with hands-on procedural involvement and working closely with investigators, CROs, and global teams to ensure high-quality study execution and regulatory compliance.
Key Responsibilities
- Assist with procedural data collection and ensure compliance with study protocols and GCP
- Support pre-study, initiation, interim, and close-out visits across multiple countries
- Engage with principal investigators and study site staff during and outside procedures
- Provide product use guidance and feedback within the operating room environment
- Monitor for device deficiencies and adverse events during live procedures
- Manage clinical supply inventory, device logistics, and reconciliation
- Assemble study binders and maintain study documentation
- Track study progress using tools such as Smartsheet and contribute to team reporting
Candidate Profile
- 3+ years’ experience supporting multi-site clinical trials in medical devices
- Functional knowledge of human anatomy and basic surgical procedures
- Comfortable working in labs and operating rooms
- Solid understanding of ISO 14155:2020, GCP, and European clinical regulations
- Proficient with Smartsheet, Adobe, EDC, and Microsoft Office applications
- Excellent communication and relationship-building skills with clinical site teams
- Able to travel 60–85% across Europe as required
Important: We are only able to consider candidates with direct clinical trial experience in medical devices. Applications from candidates with only pharmaceutical experience will not be considered.
Apply now to elevate your career and support the future of device-led clinical innovation!
Clinical Trial Assistant employer: Home Recruitment Ltd
Contact Detail:
Home Recruitment Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Assistant
✨Tip Number 1
Familiarise yourself with the specific medical device technologies your potential employer is working on. Understanding the nuances of cardiac ablation technologies will not only help you in interviews but also demonstrate your genuine interest in the role.
✨Tip Number 2
Network with professionals in the clinical trial field, especially those who have experience with medical devices. Attend industry conferences or webinars to connect with others and gain insights that could be beneficial during your application process.
✨Tip Number 3
Brush up on your knowledge of ISO 14155:2020 and GCP guidelines. Being well-versed in these regulations will not only prepare you for potential questions but also show that you are serious about compliance and quality in clinical trials.
✨Tip Number 4
Prepare to discuss your hands-on experience in clinical settings. Be ready to share specific examples of how you've supported multi-site trials and engaged with investigators, as this will highlight your practical skills and ability to work collaboratively.
We think you need these skills to ace Clinical Trial Assistant
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical trials, especially in medical devices. Emphasise your hands-on procedural involvement and any specific roles you've had in multi-site studies.
Craft a Strong Cover Letter: Write a cover letter that directly addresses the key responsibilities mentioned in the job description. Explain how your background aligns with their needs, particularly your experience with ISO 14155:2020 and GCP compliance.
Showcase Communication Skills: In your application, provide examples of how you've successfully built relationships with clinical site teams or principal investigators. This is crucial for the role, so highlight any relevant experiences.
Highlight Technical Proficiency: Mention your proficiency with tools like Smartsheet, Adobe, EDC, and Microsoft Office. If you have experience tracking study progress or managing device logistics, be sure to include that as well.
How to prepare for a job interview at Home Recruitment Ltd
✨Showcase Your Clinical Trial Experience
Make sure to highlight your 3+ years of experience in supporting multi-site clinical trials, especially in medical devices. Be prepared to discuss specific projects you've worked on and the roles you played in ensuring compliance with study protocols.
✨Demonstrate Your Knowledge of Regulations
Familiarise yourself with ISO 14155:2020 and GCP guidelines. During the interview, be ready to explain how you have applied these regulations in past roles, as this will show your understanding of the regulatory landscape.
✨Prepare for Hands-On Scenarios
Since the role involves procedural case support, think of examples where you provided guidance in an operating room or lab setting. Discuss how you interacted with investigators and site staff to ensure smooth operations during procedures.
✨Highlight Your Communication Skills
Effective communication is key in this role. Prepare to share instances where you successfully built relationships with clinical site teams or managed device logistics. This will demonstrate your ability to collaborate effectively across international sites.
