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Clinical Research Associate

LinkedIn
Greater London
2 weeks ago
Applications closed

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Clinical Research Associate

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Clinical Research Associate II

Clinical Research Associate II

Clinical Research Associate II

International Clinical Research Specialist – Cardiology Medical Device Trials


Join a medical device start-up advancing next-generation cardiac technologies through breakthrough innovation and global clinical research. With a growing European trial programme, the company is hiring an International Clinical Research Specialist to support study execution across multiple countries.


Role Overview


This fully field-based role is ideal for a clinical research professional with strong GCP knowledge and hands-on experience in medical device clinical trials. Working across Europe, you’ll play a critical role in ensuring protocol adherence, site compliance, and smooth operational delivery in partnership with CROs and internal global teams.


Extensive travel across Europe is required | Experience with medical device trials is required.


Key Responsibilities


  • Serve as the main point of contact for assigned research sites across Europe
  • Support site start-up, initiation, monitoring, and close-out activities in line with study plans
  • Ensure compliance with GCP, ISO 14155, and local regulatory requirements
  • Collaborate with investigators, study staff, CROs, and internal stakeholders to ensure high-quality execution
  • Monitor data accuracy and assist with query resolution and EDC tracking
  • Oversee device logistics, including shipments, returns, and clinical inventory
  • Manage essential documents and site binders to maintain audit readiness
  • Provide ongoing study updates and contribute to data tracking and reporting


Candidate Profile


  • Minimum 2 - 4 years’ experience in clinical research,specifically involving medical devices
  • Strong understanding of ICH-GCP, ISO 14155:2020, and European clinical trial regulations
  • Experience working with CROs and supporting multi-country site management
  • Familiarity with electronic data capture (EDC) and clinical trial management systems
  • Excellent communication and organisational skills with strong attention to detail
  • Fluent in English; additional European languages are an asset
  • Self-motivated and flexible, with the ability to travel extensively across Europe


Important:We are only able to consider candidates with clinical trial experience inmedical devices. Applications from candidates with only pharmaceutical experience will not be considered.


If you're ready to join a mission-driven team transforming cardiac care, apply now to be part of a high-impact team!

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