Clinical Research Associate I

🔥 4 minutes ago

🇩🇪 Germany – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

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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

• Support the management of clinical trial sites in compliance with ICH-GCP, study protocols, sponsor requirements, and Fortrea SOPs • Participate in site initiation, routine monitoring, and close-out visits under the guidance of experienced CRA colleagues • Conduct source data verification (SDV) and support data review activities to ensure data quality and patient safety • Assist sites with study-related questions and support issue resolution in collaboration with cross-functional teams • Maintain clinical trial documentation and support eTMF completeness and inspection readiness • Help sites meet recruitment, quality, and timeline objectives • Contribute to clinical studies across Oncology, Dermatology, Respiratory, Cardiology, and Diabetes therapeutic areas

🎯 Requirements

• Degree in Life Sciences, Nursing, Pharmacy, or a related scientific discipline • Experience in clinical research as a Study Nurse, Study Coordinator, CTA, Clinical Trial Associate, In-House CRA, or similar role • Good understanding of clinical trial processes and ICH-GCP guidelines • Strong organizational skills • Attention to detail • Proactive mindset • Fluent in German and English, both written and spoken • Willingness to travel for onsite monitoring visits across Germany

🏖️ Benefits

• Structured and supportive environment with clear development pathways and mentoring • Hands-on exposure to global clinical trials and multiple therapeutic areas • Formal training programs • Modern clinical systems • Continuous learning opportunities • Flexible work model • Competitive benefits • Culture that values collaboration, quality, and well-being