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Freelance Clinical Research Associate (CRA) Germany – Medical Devices

Belgium, Strombeek-Bever · Job Posted July 10, 2026
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Job Description

As a Freelance CRA, you will play a pivotal role in driving the success of clinical trials within the medical device sector. You will serve as the primary link between the sponsor and various investigator sites. This is a highly flexible freelance project with an average monthly resource requirement ranging from 50% to 100% of a full-time position. We welcome applicants with differing availabilities, as we may onboard two freelancers to share the project scope. Your day-to-day operations will be fully supported by a dedicated CRA Resource Manager for onboarding, while project-specific milestones will be coordinated via regular, scheduled collaboration with Clinical Trial Leaders.

Job Responsibility

  • Comprehensive Site Management: Oversee and manage investigator sites, maintaining clear and proactive communication with site staff and the sponsor
  • Full-Cycle Monitoring Visits: Independently conduct and manage all key monitoring visit types, including Site Initiation Visits, Interim Monitoring Visits, and Close-out Visits
  • Regional Travel & On-Site Presence: Execute required on-site monitoring activities and hospital visits, which are primarily situated across central, northern, and western Germany
  • Compliance & Training: Actively participate in sponsor training and ensure all clinical trial activities strictly adhere to protocols, regulatory guidelines, and quality standards
  • Reporting: Deliver clear, ad-hoc, and scheduled updates via email, telephone calls, and meetings to Clinical Trial Leaders

Requirements

  • Minimum of 5 years of clinical monitoring experience, with a proven track record of handling the main monitoring visit types (Site Qualification, Site Initiation, Interim Monitoring, and Close-Out)
  • Minimum of a Bachelor's degree within a Life Science field
  • Previous experience monitoring medical device studies is highly preferred
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