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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 medical devices.
- Benefits: Enjoy extensive travel opportunities and be part of a mission-driven team.
- Why this job: Make a real impact in healthcare while collaborating with global experts.
- Qualifications: 2-4 years in clinical research with medical devices; GCP knowledge required.
- Other info: Fluency in English is essential; additional languages are a bonus.
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 clinical research field, especially those who have experience with medical devices. Attend industry conferences or webinars to connect with potential colleagues and learn more about the latest trends in cardiology trials.
✨Tip Number 2
Familiarise yourself with the specific regulations and guidelines related to medical device trials, 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 clinical trials in detail. Be ready to share specific examples of how you've ensured protocol adherence and site compliance, as these are critical aspects of the role.
✨Tip Number 4
Highlight any experience you have working with CROs and managing multi-country sites. This will show that you can handle the complexities of international trials, which is essential for this position.
We think you need these skills to ace Clinical Research Associate
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Clinical Research Associate position. Familiarise yourself with GCP, ISO 14155, and the specifics of medical device trials.
Tailor Your CV: Highlight your relevant experience in clinical research, particularly with medical devices. Emphasise your understanding of ICH-GCP and any previous work with CROs or multi-country site management.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for advancing cardiac technologies. Mention specific experiences that demonstrate your skills in compliance, monitoring, and collaboration with stakeholders.
Proofread Your Application: Ensure your application is free from errors. A well-proofread CV and cover letter reflect your attention to detail, which is crucial in clinical research roles.
How to prepare for a job interview at Home Recruitment Ltd
✨Showcase Your GCP Knowledge
Make sure to highlight your understanding of Good Clinical Practice (GCP) during the interview. Be prepared to discuss specific examples from your past experiences where you ensured compliance with GCP guidelines in medical device trials.
✨Demonstrate Multi-Country Experience
Since this role involves extensive travel across Europe, share any relevant experiences you have managing clinical trials in multiple countries. Discuss how you navigated different regulatory environments and collaborated with diverse teams.
✨Prepare for Technical Questions
Expect technical questions related to ISO 14155 and electronic data capture (EDC) systems. Brush up on these topics and be ready to explain how you've applied this knowledge in previous roles, especially in relation to medical devices.
✨Emphasise Communication Skills
Strong communication is key in this role. Prepare to provide examples of how you've effectively communicated with investigators, CROs, and study staff. Highlight any situations where your communication skills helped resolve issues or improve study outcomes.
