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- Tasks: Support international clinical trials and ensure protocol adherence across Europe.
- Company: Join a pioneering medical device company revolutionising cardiac technology globally.
- 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 cardiology care with innovative research.
- Qualifications: Minimum 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 OverviewThe 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
- 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 or webinars to connect with potential colleagues and learn more 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'll 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 the interview by reviewing 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 in previous roles.
✨Tip Number 4
Showcase your organisational skills and attention to detail during the application process. Highlight any experience you have with data management tools and your ability to track and report on clinical trial progress, as these are crucial for the role.
We think you need these skills to ace Clinical Research Specialist
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Clinical Research Specialist position. Familiarise yourself with GCP, ICH-GCP, and ISO 14155:2020 to demonstrate your knowledge in your application.
Tailor Your CV: Highlight your relevant experience in clinical trials, particularly in medical devices or cardiology. Emphasise your skills in managing site relationships and your proficiency with EDC systems and clinical data management tools.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the company's mission. Mention specific experiences that align with the job description, such as your ability to ensure protocol compliance and support monitoring activities.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors. Ensure that your documents are clear, concise, and free from typos, as attention to detail is crucial in this field.
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 this knowledge 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 the past.
✨Prepare for Travel Discussions
Since the role involves extensive 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 trials. Prepare to discuss specific instances where your meticulous nature has positively impacted data accuracy, protocol adherence, or site compliance in your previous roles.
