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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 medical advancements.
- 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 applicable.
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
Network with professionals in the medical device industry, especially those who have experience in clinical trials. Attend relevant conferences or webinars to meet potential colleagues and learn more about the field.
✨Tip Number 2
Familiarise yourself with the latest developments in cardiac ablation technologies. This knowledge will not only help you during interviews but also demonstrate your genuine interest in the role and the company.
✨Tip Number 3
Prepare to discuss specific examples from your previous clinical trial experiences that highlight your problem-solving skills and ability to work under pressure, especially in operating room settings.
✨Tip Number 4
Showcase your proficiency with tools like Smartsheet and Microsoft Office by being ready to discuss how you've used them in past roles to manage data and track project progress effectively.
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 Compelling Cover Letter: Write a cover letter that showcases your passion for clinical trials and your understanding of the cardiac ablation technologies. Mention your familiarity with ISO 14155:2020 and GCP, and how your skills align with the job requirements.
Highlight Relevant Skills: In your application, clearly outline your proficiency with tools like Smartsheet and Microsoft Office. Also, mention your communication skills and ability to build relationships with clinical site teams, as these are crucial for the role.
Showcase Your Experience: Provide specific examples of your past experiences in clinical trials, particularly any roles involving device logistics or procedural data collection. This will demonstrate your capability and readiness for the responsibilities outlined in the job description.
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, GCP, and European clinical regulations. During the interview, be ready to explain how you have applied these standards in your previous roles to ensure high-quality study execution.
✨Prepare for Hands-On Scenarios
Since this role involves procedural case support, think about how you would handle real-life scenarios in the operating room. Be ready to discuss your comfort level with surgical procedures and how you would provide product use guidance during live procedures.
✨Emphasise Communication Skills
Strong communication and relationship-building skills are crucial for this position. Prepare examples of how you've effectively engaged with principal investigators and study site staff, both during and outside of procedures, to foster collaboration and ensure smooth operations.
