
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.
🔥 21 hours ago
🌵 Arizona, North Carolina, +1 more states – Remote
💵 $16 - $33 / hour
⏰ Full Time
🟢 Junior
🟡 Mid-level
🦅 H1B Visa Sponsor
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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.
• Provide administrative and project tracking support to the clinical project team • Ensure assigned project tasks with Project Delivery services are performed timely and accurately • Arrange and track system access for project team members • Maintain and quality audit project portal documents to ensure current revisions are available • Assist with preparation and shipment of clinical trial documentation, including Investigator Site File • Maintain version and quality control of project documentation and submit it to the trial master file • Track and maintain project-related information, including the site medical question and answer log
• Excellent written and verbal English • Fluency in 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 • Degree level qualification or equivalent experience • Minimum of one years’ experience in a related role • Skill sets and proven performance equivalent to the above
• Competitive benefits package depending on location • Transparent compensation and pay equity
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