
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.
🔥 0 minutes ago
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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 completed timely and accurately • Arrange and track system access for project team members • Maintain and quality audit project portal documents to ensure current revisions • Assist with preparation and shipment of clinical trial documentation, including Investigator Site Files • Maintain version control and quality control of project documentation • Submit project documentation 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 year of experience in a related role • Skill sets and proven performance equivalent to the above
• Diverse and inclusive work environment • Supportive and cohesive teams • Accessible, hands-on leaders • Equal employment opportunities • Exceptional employee experiences • Collaboration and creativity-focused workplace
Apply Now🕒 5 days ago
Site Payments Associate configuring accurate, timely clinical trial payments for Parexel, a global CRO. Reviewing contracts, budgets, payment data, and site documentation across Argentina and Mexico.
🕒 July 25
M&A Origination Associate in Latin America identifying and building relationships with small and mid-sized businesses. Conducting research-heavy outreach to qualify opportunities and hand off to investment team.
🗣️🇪🇸 Spanish Required
🗣️🇧🇷🇵🇹 Portuguese Required
🕒 July 23
Site Management Associate supporting international clinical research projects by streamlining communication and managing documentation. Coordinating regulatory submissions and assisting in pre-study site testing.
🕒 July 15
Site Contract Associate responsible for negotiation and execution of site contracts for clinical trials at Parexel. Contributing to a global clinical research team working remotely from Argentina, Mexico, or Brazil.