Clinical Research Associate

Home Recruitment Ltd; Birmingham; On-site; GBP 35,000 - 55,000; Full time

Job summary

A medical device start-up is seeking an International Clinical Research Specialist to advance cardiac technologies through global clinical research. This fully field-based role involves managing clinical trials across Europe, ensuring protocol adherence and operational delivery. Candidates require experience with medical devices, GCP knowledge, and excellent communication skills.

Qualifications

• 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.

Responsibilities

• Serve as the main point of contact for assigned research sites across Europe.
• Support site start-up, initiation, monitoring, and close-out activities.
• Ensure compliance with GCP, ISO 14155, and local regulatory requirements.

Skills

Communication

Organisational skills

Attention to detail

GCP knowledge

Experience with medical devices

Tools

Electronic data capture (EDC)

Clinical trial management systems

Job description

Direct message the job poster from Home Recruitment Ltd

Executive Recruiter | UK | EMEA | APAC | USA

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 in medical 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!

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  General Business, Health Care Provider, and Research

• Industries

  Medical Equipment Manufacturing

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