Clinical Research Associate – DACH

🔥 2 hours ago

🇩🇪 Germany – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Fortrea

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.

📋 Description

• Identify and assess new potential investigators and sites • Recommend sites during feasibility and selection phases • Conduct pre-study, initiation, monitoring, and close-out visits • Monitor site performance, data quality, and protocol compliance • Act as a key point of contact for site personnel, providing training and support • Use data insights to assess risks and drive decisions • Support regulatory audits, EC submissions, and system access coordination

🎯 Requirements

• University or college degree in life sciences, nursing, pharmacy, or a related allied health profession; equivalent relevant experience may be considered in lieu of formal education • Basic to good knowledge of ICH/GCP Guidelines and applicable local laws and regulations governing clinical trials • Solid understanding of clinical research processes, regulations, and methodology • Strong organizational and time management skills • Ability to build and maintain relationships • 1 to 3 years of monitoring experience required within CRO or Pharma environment

🏖️ Benefits

• Regional monitoring—minimizing travel while maximizing your impact • Supportive environment • Opportunity to contribute to meaningful research that improves lives • Sponsor-dedicated team with a strong pipeline and purpose