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For Companies At a Glance
- Tasks: Support international clinical trials in cardiology, ensuring compliance and data accuracy.
- Company: Join a pioneering medical device company revolutionising cardiac technology across Europe.
- Benefits: Enjoy flexible working, travel opportunities, and the chance to make a real impact.
- Why this job: Be part of a mission-driven team transforming healthcare with innovative solutions.
- Qualifications: 4+ years in clinical trials, strong GCP knowledge, and excellent communication skills required.
- Other info: Fluency in English is essential; additional languages are a plus.
The predicted salary is between 36000 - 60000 £ per year.
This is a rare opportunity to join a pioneering medical device company bringing next-generation cardiac technology to the global stage. With an expanding European trial programme and breakthrough innovation at its core, the business is now seeking an International Clinical Research Specialist to support study execution across multiple European countries.
This fully field-based role is ideal for a clinical research professional with a strong understanding of GCP and experience supporting medical device or cardiology studies. Working across Europe, you’ll play a vital role in ensuring protocol adherence, site compliance, and smooth operational delivery in collaboration with global clinical teams and CRO partners.
Role Overview
The Clinical Research Specialist will support the planning, implementation, and oversight of international clinical trials. You will liaise with investigators, support monitoring activities, ensure data accuracy, and uphold ethical and regulatory standards at each site. Applicants must be open to regular travel across Europe.
Key Responsibilities
- Provide clinical case support and serve as the key contact for research sites across Europe
- Liaise with PIs, study staff, CROs, and other stakeholders to ensure protocol compliance
- Attend site visits, including initiation, interim, and close-out, in line with the Monitoring Plan
- Support remote and on-site monitoring activities, including query resolution and data validation
- Ensure accurate tracking and reporting of adverse events in compliance with local regulations
- Coordinate logistics, device shipment and returns, and maintain clinical supply inventory
- Assemble, distribute, and manage site binders and study-specific documentation
- Contribute to data tracking, reporting, and study updates using clinical data management tools
Candidate Profile
- Minimum 4 years’ experience supporting clinical trials, ideally in medical devices or cardiology
- Strong knowledge of ICH-GCP, ISO 14155:2020, and international clinical research regulations
- Experience working with CROs and managing site relationships across multiple countries
- Proficient in Microsoft Office, with hands-on experience using EDC systems and clinical data management platforms
- Exceptional communication and organisational skills, with a strong attention to detail
- Fluent English is essential; additional European languages are a strong advantage
- Flexible, self-driven, and comfortable with extensive travel
If you’re ready to join a mission-driven company transforming cardiology care, apply now and join a high-impact team driving clinical research innovation across Europe.
Clinical Research Specialist employer: Home Recruitment Ltd
Contact Detail:
Home Recruitment Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Specialist
✨Tip Number 1
Network with professionals in the clinical research field, especially those who have experience in cardiology or medical devices. Attend industry conferences and seminars to meet potential colleagues and learn about the latest trends in clinical trials.
✨Tip Number 2
Familiarise yourself with the specific regulations and guidelines related to clinical trials in the European countries where you will be working. This knowledge will not only help you during interviews but also demonstrate your commitment to compliance and protocol adherence.
✨Tip Number 3
Prepare for interviews by practising answers to common questions related to clinical trial management and your experience with GCP and ISO standards. Be ready to discuss specific examples of how you've ensured protocol compliance and managed site relationships.
✨Tip Number 4
Showcase your organisational skills and attention to detail during the interview process. You might be asked to describe how you manage multiple tasks and ensure data accuracy, so have examples ready that highlight your ability to juggle responsibilities effectively.
We think you need these skills to ace Clinical Research Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trials, particularly in medical devices or cardiology. Emphasise your understanding of GCP and any specific achievements that demonstrate your expertise.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your motivation to work with the pioneering medical device company. Mention your experience with international trials and how you can contribute to their mission.
Highlight Language Skills: If you speak additional European languages, be sure to mention them prominently in your application. This could set you apart from other candidates and show your ability to communicate effectively across diverse teams.
Showcase Your Organisational Skills: In your application, provide examples of how you've successfully managed multiple tasks or projects in previous roles. Highlight your attention to detail and ability to maintain compliance with regulations, as these are crucial for the role.
How to prepare for a job interview at Home Recruitment Ltd
✨Showcase Your Clinical Knowledge
Make sure to highlight your understanding of GCP, ICH-GCP, and ISO 14155:2020 during the interview. Be prepared to discuss how you've applied these regulations in previous roles, especially in medical device or cardiology studies.
✨Demonstrate Your Communication Skills
As a Clinical Research Specialist, you'll be liaising with various stakeholders. Use the interview to showcase your exceptional communication skills by providing examples of how you've effectively collaborated with investigators, CROs, and study staff in past projects.
✨Prepare for Travel Discussions
Since the role involves regular travel across Europe, be ready to discuss your flexibility and experience with travel. Share any relevant experiences that demonstrate your ability to manage logistics and maintain productivity while on the move.
✨Emphasise Attention to Detail
Attention to detail is crucial in clinical research. Prepare to discuss specific instances where your meticulous nature has positively impacted study outcomes, such as ensuring data accuracy or managing site compliance effectively.
