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- Tasks: Support clinical trials by managing logistics, collecting data, and ensuring compliance across international sites.
- Company: Join a pioneering company developing next-gen cardiac ablation technologies.
- Benefits: Enjoy a full-time role with opportunities for travel and hands-on experience in the medical field.
- Why this job: Be part of innovative clinical research that impacts patient care and device-led advancements.
- Qualifications: 3+ years in medical device trials, knowledge of human anatomy, and proficiency in relevant software.
- Other info: Candidates must have direct clinical trial experience; pharmaceutical backgrounds won't be considered.
The predicted salary is between 36000 - 60000 £ per year.
Direct message the job poster from Home Recruitment Ltd
Executive Recruiter | UK | EMEA | APAC | USA
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!
Seniority level
-
Seniority level
Mid-Senior level
Employment type
-
Employment type
Full-time
Job function
-
Job function
Administrative, Research, and Health Care Provider
-
Industries
Medical Equipment Manufacturing and Hospitals and Health Care
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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
Make sure to highlight your hands-on experience in clinical trials, especially with medical devices. When you connect with the job poster or during networking, emphasise specific instances where you've successfully managed device logistics or supported procedures.
✨Tip Number 2
Familiarise yourself with the latest regulations and guidelines, such as ISO 14155:2020 and GCP. Being able to discuss these in detail will show your commitment to compliance and quality in clinical trials, which is crucial for this role.
✨Tip Number 3
Engage with professionals in the field through platforms like LinkedIn. Join groups related to clinical trials and medical devices, and participate in discussions to build your network and gain insights that could be beneficial during your application process.
✨Tip Number 4
Prepare to discuss your experience with tools like Smartsheet and Microsoft Office during any informal chats or interviews. Being proficient with these tools is essential for tracking study progress and managing documentation effectively.
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 achievements that align with the job description.
Craft a Compelling Cover Letter: Write a cover letter that directly addresses the key responsibilities mentioned in the job description. Explain how your background in managing device logistics and supporting multi-site trials makes you an ideal candidate for this role.
Highlight Relevant Skills: In your application, clearly outline your proficiency with tools like Smartsheet and Microsoft Office, as well as your understanding of ISO 14155:2020 and GCP. These skills are crucial for the role and should be prominently featured.
Showcase Communication Abilities: Since excellent communication and relationship-building skills are essential, provide examples in your application of how you've successfully engaged with clinical site teams or principal investigators in past roles.
How to prepare for a job interview at Home Recruitment Ltd
✨Know Your Clinical Trial Basics
Make sure you have a solid understanding of clinical trial processes, especially in the context of medical devices. Brush up on ISO 14155:2020 and GCP guidelines, as these will likely come up during your interview.
✨Demonstrate Hands-On Experience
Be prepared to discuss your hands-on experience in operating rooms and labs. Share specific examples of how you've supported procedures and engaged with investigators, as this role requires practical involvement.
✨Showcase Your Communication Skills
Since this role involves working closely with various stakeholders, highlight your communication and relationship-building skills. Prepare examples of how you've effectively collaborated with clinical site teams in the past.
✨Prepare for Travel Discussions
Given the travel requirements of 60-85%, be ready to discuss your flexibility and willingness to travel. It’s important to convey that you’re comfortable with the demands of an international role.
