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.

Clinical Research Specialist – Cardiology Trials (International)

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 based within the EU and open to regular travel.

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.

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