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- Tasks: Support clinical trials across Europe, ensuring compliance and smooth operations.
- Company: Join a start-up revolutionising cardiac technologies through innovative research.
- Benefits: Enjoy extensive travel opportunities and be part of a mission-driven team.
- Why this job: Make a real impact in healthcare while working with cutting-edge medical devices.
- Qualifications: 2-4 years in clinical research, specifically with medical devices, is essential.
- Other info: Fluency in English required; additional languages are a plus.
The predicted salary is between 36000 - 60000 £ per year.
Join a medical device start-up advancing next-generation cardiac technologies through breakthrough innovation and global clinical research. With a growing European trial programme, the company is hiring an International Clinical Research Specialist to support study execution across multiple countries.
This fully field-based role is ideal for a clinical research professional with strong GCP knowledge and hands-on experience in medical device clinical trials. Working across Europe, you’ll play a critical role in ensuring protocol adherence, site compliance, and smooth operational delivery in partnership with CROs and internal global teams. Extensive travel across Europe is required; experience with medical device trials is required.
Key Responsibilities- Serve as the main point of contact for assigned research sites across Europe
- Support site start-up, initiation, monitoring, and close-out activities in line with study plans
- Ensure compliance with GCP, ISO 14155, and local regulatory requirements
- Collaborate with investigators, study staff, CROs, and internal stakeholders to ensure high-quality execution
- Monitor data accuracy and assist with query resolution and EDC tracking
- Oversee device logistics, including shipments, returns, and clinical inventory
- Manage essential documents and site binders to maintain audit readiness
- Provide ongoing study updates and contribute to data tracking and reporting
- Minimum 2 - 4 years’ experience in clinical research, specifically involving medical devices
- Strong understanding of ICH-GCP, ISO 14155:2020, and European clinical trial regulations
- Experience working with CROs and supporting multi-country site management
- Familiarity with electronic data capture (EDC) and clinical trial management systems
- Excellent communication and organisational skills with strong attention to detail
- Fluent in English; additional European languages are an asset
- Self-motivated and flexible, with the ability to travel extensively across Europe
Important: We are only able to consider candidates with clinical trial experience in medical devices. Applications from candidates with only pharmaceutical experience will not be considered.
If you’re ready to join a mission-driven team transforming cardiac care, apply now to be part of a high-impact team!
Clinical Research Associate employer: Home Recruitment Ltd
Contact Detail:
Home Recruitment Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate
✨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 connect with potential colleagues and learn more about the latest trends in cardiology.
✨Tip Number 2
Familiarise yourself with the specific regulations and guidelines related to medical device trials in Europe, such as ISO 14155 and ICH-GCP. This knowledge will not only boost your confidence but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Prepare to discuss your hands-on experience with site management and monitoring during interviews. Be ready to share specific examples of how you've ensured protocol adherence and site compliance in previous roles.
✨Tip Number 4
Highlight any experience you have with electronic data capture (EDC) systems and clinical trial management systems. Being able to speak confidently about these tools can set you apart from other candidates.
We think you need these skills to ace Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical research, particularly with medical devices. Emphasise your understanding of GCP, ISO 14155, and any specific trials you've worked on.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for cardiac technologies and your experience in multi-country site management. Mention specific examples of how you've ensured protocol adherence and compliance in previous roles.
Highlight Language Skills: If you speak any additional European languages, be sure to mention them in your application. This can set you apart from other candidates and is particularly valuable for a role that involves extensive travel across Europe.
Showcase Communication Skills: In your application, provide examples of how you've effectively communicated with investigators, study staff, and CROs. Strong communication skills are essential for this role, so make sure to highlight your ability to collaborate and resolve queries.
How to prepare for a job interview at Home Recruitment Ltd
✨Showcase Your Clinical Research Experience
Be prepared to discuss your previous roles in clinical research, especially those involving medical devices. Highlight specific projects you've worked on, focusing on your contributions and the outcomes achieved.
✨Demonstrate GCP Knowledge
Since the role requires a strong understanding of Good Clinical Practice (GCP), be ready to explain key principles and how you've applied them in past trials. This will show your familiarity with regulatory standards.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world situations. Think of examples where you had to ensure protocol adherence or resolve compliance issues, and be ready to discuss your approach.
✨Emphasise Communication Skills
As this role involves collaboration with various stakeholders, highlight your communication and organisational skills. Share examples of how you've effectively communicated with investigators, CROs, and study staff in previous roles.
