Clinical Trials Associate – Serbia, UK, Poland, Spain

🔥 7 minutes ago

🌐 Serbia, United Kingdom, +2 more countries – Remote

🇷🇸 Serbia – Remote 🇬🇧 United Kingdom – Remote 🇵🇱 Poland – Remote 🇪🇸 Spain – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Associate

🚫👨‍🎓 No degree required

👻 Ghost score 10%

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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

• Coordinate and track system access for project team members • Maintain project portals and perform quality checks to ensure current document revisions are available • Support preparation and shipment of clinical trial documentation, including Investigator Site Files • Maintain version and quality control of project documentation and submit documentation to the Trial Master File • Track and maintain key project information, including site medical question and answer logs and current site and personnel details • Prepare and distribute meeting minutes for Sponsor and Internal Management meetings • Coordinate and track distribution of project-specific training • Provide additional administrative and project support as assigned • Collaborate with Project Managers, Lead CRAs, CRAs, and other project team members across assigned clinical trials

🎯 Requirements

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

🏖️ Benefits

• Collaborative and inclusive work environment • Growth and learning opportunities • Career development opportunities • Remote work arrangement • No travel required

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