Clinical Trials Associate

🔥 0 minutes ago

🏈 Alabama, Arizona, +2 more states – Remote

🏈 Alabama – Remote 🌵 Arizona – Remote ⛰️ Colorado – Remote 🌲 North Carolina – Remote

💵 $16 - $33 / hour

⏰ Full Time

🟢 Junior

🟡 Mid-level

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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 • 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 Files • Maintain version control and quality control of project documentation and submit documentation to the trial master file • Track and maintain project-related information, including site medical question and answer logs • Generate and distribute minutes for Sponsor and Internal Management meetings • Maintain current participating site and personnel information • Arrange and track distribution of project-specific training to project teams • Perform other duties as assigned

🎯 Requirements

• Degree level qualification or equivalent experience • Minimum of one years’ experience in a related role • 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 • Sense of urgency and adaptability in a fast-paced, rapidly changing environment • 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 • Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations, as applicable

🏖️ Benefits

• Competitive benefits package depending on location • Transparent compensation and pay equity • Inclusive and equitable workplace