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- 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 globally.
- Qualifications: 3+ years in medical device trials; knowledge of anatomy and surgical procedures required.
- Other info: Candidates must have direct clinical trial experience in medical devices.
The predicted salary is between 36000 - 60000 £ per year.
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 Specialist employer: Home Recruitment Ltd
Contact Detail:
Home Recruitment Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Specialist
✨Tip Number 1
Familiarise yourself with the latest advancements in cardiac ablation technologies. Understanding the specifics of the devices you'll be working with will not only boost your confidence but also impress potential employers during discussions.
✨Tip Number 2
Network with professionals in the medical device industry, especially those involved in clinical trials. Attend relevant conferences or webinars to connect with key players and gain insights that could give you an edge in your application.
✨Tip Number 3
Brush up on your knowledge of ISO 14155:2020 and GCP guidelines. Being well-versed in these regulations will demonstrate your commitment to compliance and quality in clinical trials, making you a more attractive candidate.
✨Tip Number 4
Prepare to discuss your hands-on experience in operating rooms and labs. Be ready to share specific examples of how you've supported clinical trials, as this practical knowledge is crucial for the role and will set you apart from other applicants.
We think you need these skills to ace Clinical Trial Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical trials, particularly in medical devices. Emphasise your hands-on procedural involvement and any specific projects that align with the responsibilities outlined in the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical trials and your understanding of cardiac ablation technologies. Mention your familiarity with GCP and ISO 14155:2020, and how your skills can contribute to the company's goals.
Highlight Relevant Skills: In your application, clearly outline your proficiency with tools like Smartsheet and Microsoft Office. Discuss 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 previous work in multi-site clinical trials. Detail your experience with device logistics, data collection, and compliance with study protocols to demonstrate your suitability for the position.
How to prepare for a job interview at Home Recruitment Ltd
✨Know Your Clinical Trial Basics
Make sure you brush up on your knowledge of clinical trials, especially in the medical device sector. Understand the key regulations like ISO 14155:2020 and GCP, as well as the specific protocols related to cardiac ablation technologies.
✨Showcase Your Hands-On Experience
Be prepared to discuss your hands-on experience in operating rooms and labs. Highlight any specific instances where you've provided procedural support or engaged with investigators, as this will demonstrate your comfort level in high-pressure environments.
✨Demonstrate Strong Communication Skills
Since this role involves working closely with various stakeholders, emphasise your communication and relationship-building skills. Share examples of how you've successfully collaborated with clinical site teams or managed logistics in previous roles.
✨Prepare for Travel Discussions
Given the travel requirements of the position, be ready to discuss your flexibility and willingness to travel across Europe. It’s a good idea to have a plan in mind for how you would manage your schedule and commitments while on the road.