Clinical Trials Associate

🔥 4 minutes ago

🌐 Argentina, Mexico, +1 more countries – Remote

🇦🇷 Argentina – Remote 🇲🇽 Mexico – Remote 🇧🇷 Brazil – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Associate

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Provide administrative and project-tracking support to clinical project teams • Coordinate and track system access for Project Managers, Lead CRAs, and CRAs • Maintain project portals and perform quality checks on document versions • Support preparation, shipment, version control, and filing of clinical trial documentation, including Investigator Site Files and Trial Master File documentation • Track project information, including site medical question and answer logs and participating site and personnel details • Prepare and distribute meeting minutes for sponsor, project, and internal management meetings • Coordinate and track project-specific training • Support timely and accurate administrative activities contributing to effective clinical trial delivery • Collaborate with Project Managers, Lead CRAs, CRAs, and other global team members across multiple time zones

🎯 Requirements

• Degree-level qualification or equivalent experience • Minimum of one year of experience in a related role • Proficiency in English, written and verbal • Fluency in the language of the country where the role is located • Knowledge and understanding of ICH, GCP, and applicable FDA or EU directive regulations • Strong organizational, problem-solving, and interpersonal skills • Excellent attention to detail and quality • Ability to work independently and collaboratively as part of a team • Ability to manage multiple priorities, exercise independent judgment, and adapt effectively in a fast-paced, changing environment • Excellent skills in Microsoft Office applications, including Outlook, Word, Excel, and PowerPoint

🏖️ Benefits

• Collaborative and inclusive environment • Growth and career development opportunities • Opportunity to learn and grow • Meaningful work improving patients’ lives through clinical research