Clinical Trial Specialist

Home Recruitment Ltd; United Kingdom; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading company in the medical device sector is seeking a Clinical Trial Support Specialist for an international role. The ideal candidate will oversee procedural case support and manage device logistics while ensuring compliance with study protocols across multiple countries. This position offers the opportunity to work closely with investigators and contribute to the future of cardiac ablation technologies.

Qualifications

• 3+ years’ experience in supporting multi-site clinical trials.
• Functional knowledge of human anatomy and surgical procedures.
• Solid understanding of ISO 14155:2020 and GCP.

Responsibilities

• Assist with procedural data collection and ensure compliance with study protocols.
• Support pre-study, initiation, interim, and close-out visits.
• Monitor device deficiencies and adverse events during procedures.

Skills

Excellent communication

Relationship-building

Regulatory compliance

Tools

Smartsheet

Adobe

EDC

Microsoft Office

Job description

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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