Clinical Trials Associate

🕒 September 15

🇰🇷 South Korea – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Associate

👻 Ghost score 15%

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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

• Arrange and track system access for project team members • Maintain and quality audit current document revisions on project portals • 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 site medical question and answer logs • Generate and distribute minutes for project-related meetings, including Sponsor and Internal Management meetings • Maintain current participating site and personnel information • Arrange and track project-specific training distribution to the project team • Perform other assigned duties

🎯 Requirements

• Degree level qualification or equivalent experience • Minimum of one year of experience in a related role • Skill sets and proven performance equivalent to the stated requirements • Excellent written and verbal English • Fluency in the language of the country of location • Strong interpersonal skills • Ability to work independently and as a team member • Ability to adapt in a fast-paced and rapidly changing environment • Ability to handle multiple tasks and exercise independent judgment • Strong attention to detail and focus on quality • Strong organizational and problem-solving skills • Excellent MS Office skills, including Outlook, Word, Excel and PowerPoint • Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations, as applicable

🏖️ Benefits

• Equal employment opportunities regardless of protected characteristics • Diverse and inclusive work environment • Supportive and collaborative teams • Accessible leadership • Employee opportunities to succeed and thrive

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