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Fortrea

Unblinded CRA based in Germany (Ruhrgebiet)

Munich · Remote Germany

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hirly's read of this role

Seniority
Mid level
Country
DE
Work mode
On-site / unstated
First seen by hirly
1 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Join a sponsor-dedicated model supporting cutting-edge clinical trials in DACH. As an unblinded Clinical Research Associate (CRA I or CRA II level) , you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a collaborative global environment.

Key Responsibilities

  • You will perform unblinded monitoring activities in line with ICH-GCP guidelines and applicable regulations, including Investigational Product oversight
  • You will ensure protocol compliance, data integrity, and patient safety at assigned sites
  • You will maintain accurate and complete study documentation, including eTMF and regulatory files
  • You will build strong relationships with site staff, acting as the primary point of contact for site management (pharmacy only)
  • You could contribute to audit readiness and ensure inspection preparedness at site level

Required Qualifications

  • Bachelor’s degree in Life Sciences or related field (or equivalent experience)
  • Initial experience in clinical research as a CRA with at least 1 year of monitoring experience
  • Understanding of ICH-GCP guidelines and clinical trial processes
  • Strong interest and knowledge in unblinded study conduct and Investigational Product management
  • Fluency in German and English (written and spoken)
  • Willingness to travel within Germany and Austria as required
  • Strong organizational skills with attention to detail

What We Offer

  • Opportunity to work in a sponsor-dedicated environment on innovative studies
  • Structured onboarding and continuous development programs
  • Flexible working model supporting work-life balance
  • Access to global career growth opportunities within clinical operations
  • Inclusive and collaborative culture with employee resource groups and wellbeing initiatives

If you are looking to build your clinical monitoring career within a high-impact and supportive environment, we encourage you to apply and grow with us.

#LI-GQ1 #LI-Remote

Learn more about our EEO & Accommodations request here .

Original posting on Fortrea's site ↗

Listed on hirly, a job board. hirly is not the employer: Fortrea is hiring for this role.

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