
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.
🔥 12 hours ago
🌐 United States, Canada – Remote
🌵 Arizona, Colorado, +2 more states – Remote
💵 $16 - $33 / hour
⏰ Full Time
🟢 Junior
🟡 Mid-level
🦅 H1B Visa Sponsor
👻 Ghost score 0%
Where this job comes from
Posted on Worldwide Clinical Trials's careers page, not through a job board
First seen by Remote Rocketship 12 hours ago
Still open on Worldwide Clinical Trials's site. Checked 1 hour ago.

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.
• 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
• 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 • Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role • Skill sets and proven performance equivalent to the above
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