
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.
🔥 2 hours ago
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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.
• Lead and oversee clinical data management activities across multiple complex global studies from start-up through closeout • Coordinate resources to ensure data management deliverables are completed on time and within budget • Develop and maintain trial documentation, including data management plans, database specifications, edit check specifications, and related study materials • Drive effective user acceptance testing (UAT) for database builds and study execution • Manage vendor data reconciliation activities and define specifications for reconciliation outputs • Oversee data cleaning to ensure accurate, complete, and reliable clinical trial data • Monitor study progress through key metrics, identify risks, and communicate concerns to data management leadership • Partner with internal and external stakeholders in study meetings and cross-functional discussions • Lead or contribute to process reviews and continuous improvement initiatives
• Bachelor's degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, or equivalent relevant experience • Minimum 3 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries • Working knowledge of clinical data management best practices and technologies used in clinical trials
• Diverse and inclusive work environment • Collaborative and supportive teams • Accessible leadership • Equal employment opportunities • Employee experiences where everyone is respected and has access to equal opportunity
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