Worldwide Clinical Trials
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.
Clinical Research Associate – Oncology, Hematology, CNS, Cardiometabolic
🕒 June 25
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Worldwide Clinical Trials
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
• Responsible for site qualification, initiation, interim monitoring, site management, and study close-out visits • Document site visit findings via written reports • Assess, monitor, and train study site staff on protocol adherence
🎯 Requirements
• 2+ years of experience as a Clinical Research Associate • 4-year university degree or RN/BSN in Nursing • Experience in Hematology, Oncology, Neurology or Cardiometabolic
🏖️ Benefits
• Diverse and inclusive work environment • Mentoring and guidance for CRAs • Extensive support for regulatory submissions • Collaboration with top-tier colleagues • Opportunity to impact patients' lives
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