Worldwide Clinical Trials
1001 - 5000 employees
🧬 Biotechnology
đź’Š 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.
Senior Clinical Trials Associate
🔥 0 minutes ago
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Worldwide Clinical Trials
1001 - 5000 employees
🧬 Biotechnology
đź’Š 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.
đź“‹ Description
• Provide administrative and project tracking support to the clinical project team • Arrange and track system access for project team • Maintain and quality audit to assure the most recent revisions of documents are on project portals • Assist project team with preparation and shipment of clinical trial documentation • Maintain version and quality control of project documentation • Generate and distribute minutes for project related meetings • Maintain current participating site and personnel information • Assist with the interviewing, coaching, training and development of new employees • Participate in special and complex projects to continuously improve processes
🎯 Requirements
• Degree level qualification or equivalent experience • Minimum of two years’ experience in a related role • Strong attention to detail and quality of work • Excellent written and verbal English skills • Strong organizational and problem-solving skills • Proficient in MS Office applications including Outlook, Word, Excel and PowerPoint • Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)
🏖️ Benefits
• Inclusive and diverse work environment • Opportunities for professional development • Training and coaching for new employees • Collaborative team culture
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