Clinical Trials Associate

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Worldwide Clinical Trials

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.

📋 Description

• Provide administrative and project tracking support to the clinical project team • Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.) • 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, including Investigator Site File • Maintain version and quality control of project documentation and submit to trial master file • Assist with the tracking and maintenance of project related information, including site medical question and answer log

🎯 Requirements

• Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role • Excellent written and verbal English as well as fluency of the language of the country of location • Ability to handle multiple tasks and exercise independent judgment • Strong attention to detail and focus on quality of work • Strong organizational and problem-solving skills • Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint

🏖️ Benefits

• Flexible working arrangements • Professional development • Diverse and inclusive work environment

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