Worldwide Clinical Trials
1001 - 5000 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
Clinical Trials Associate
🕒 May 26
📊 Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
Worldwide Clinical Trials
1001 - 5000 employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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 the clinical project team • Ensure tasks for all assigned projects are performed timely and accurately • Arrange and track system access for project team members • Maintain and quality audit project documentation • Assist project team with preparation and shipment of clinical trial documentation • Maintain version and quality control of project documentation • Submit to trial master file • Track and maintain project related information • Generate and distribute minutes for project related meetings • Maintain current participating site and personnel information • Arrange and track distribution of project specific training to project team • Perform other duties as assigned
🎯 Requirements
• Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role • Excellent written and verbal English as well as fluency of the language of the country of location • Strong interpersonal skills • Ability to work independently and as a team member • Sense of urgency and ability to be adaptable 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 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
• Global team events • Diverse and inclusive environment • Professional development opportunities
Apply Now
