
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.
• Responsible for the overall coordination and management of clinical trials from start-up through closeout activities • Directs the technical, financial and operational aspects of the projects • Works with major functional area leads to identify and evaluate fundamental issues on the project • Interpret data on complex issues, make good business decisions and ensure solutions are implemented • Ensure that all project deliverables meet the customer’s time/quality/cost expectations • Accountable for ensuring that all project deliverables meet the customer/contract expectations
• 5 years' industry experience with previous experience in a Clinical Project Management role, within a CRO setting • University/College degree, within Life Science is preferred • Experience managing Oncology studies is required for this role • Ability to travel when needed • Excellent interpersonal, oral, and written communication skills in English • Superior planning and organizational skills with attention to details • Proficiency in Microsoft Office, CTMS and EDC Systems
• Cultivating a diverse and inclusive environment • Committed to enabling professionals from all backgrounds and experiences to succeed
Apply Now🕒 2 days ago
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