
1001 - 5000 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
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1001 - 5000 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
• Oversee, lead, manage and provide technical expertise within the assigned complex projects/programs • Provide subject matter expert support, solution management and departmental support for project initiatives and training • Provide fully independent and autonomous leadership of data management services across multiple complex global projects/programs • Liaise with DM Management at regular intervals • Collaborate with internal WCT departments working on the same project • Provide mentorship to other members of the DM department • Participate in sponsor audits, regulatory authority inspections and other third party meetings
• Bachelor’s degree or higher in biomedical sciences, life sciences, computer science or related discipline — or equivalent relevant experience • Min of 7 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries.
• competitive benefits package depending on location • pay equity and transparency • compliance with applicable labor laws
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