CRA II – Oncology, Neurology

🕒 October 1

🇩🇪 Germany – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Conduct site qualification, initiation, monitoring, and close-out visits in compliance with study protocols and regulatory requirements • Evaluate site feasibility and support site selection activities for new and ongoing studies • Review source documentation and study data to ensure accuracy, patient safety, protocol compliance, and data integrity • Prepare, maintain, and verify regulatory and ethics documentation required for study conduct • Train and support site personnel on protocol requirements, study processes, and GCP standards • Partner with investigative sites to resolve data queries, maintain study documentation, and support audit readiness • Monitor investigational product accountability, including receipt, storage, return, or destruction activities • Document site visit findings and provide timely updates and essential documentation for Trial Master File maintenance • Collaborate with study teams and support the development of monitoring-related study materials and processes as requested • Support sites across Germany while traveling to investigative sites approximately 6–8 days per month

🎯 Requirements

• Medical Doctor (MD) degree, Pharmacy degree, or equivalent life science qualification with the required clinical research experience; or a four-year degree in a medical, biological, physical, health, pharmacy, or related scientific discipline with clinical research experience • Minimum experience requirements consistent with a CRA II level role, including prior experience in clinical research and site monitoring activities • Thorough understanding of clinical research processes, GCP, ICH guidelines, FDA and/or EU regulations, and local regulatory requirements • Experience managing investigative sites through study start-up, monitoring, and close-out activities • Knowledge of multiple therapeutic areas and ability to independently support clinical trial execution • Proficiency with Microsoft Office, electronic data capture (EDC) systems, and IxRS platforms • Fluent in German and proficient in spoken and written English • Valid passport and driving license • Willingness to travel • Candidates must reside in Germany

🏖️ Benefits

• Equal employment opportunities regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law • Supportive and cohesive teams • Diverse and inclusive work environment • Home-based work arrangement

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