
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.
🕒 April 29
Improve your chances of getting an interview by checking your resume score before you apply.

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.
• Responsible for site qualification, initiation, interim monitoring, site management, and study close-out visits • Document site visit findings via written reports • Conduct source document verification for compliance, patient safety, and veracity of data • Review study subject safety information and informed consent
• 2+ years of experience as a Clinical Research Associate • 4-year university degree or RN/BSN in Nursing • Experience in Hematology, Oncology and Cardiometabolic (Obesity, T1D/T2D, GLP) is required • Proficiency in Microsoft Office, CTMS and EDC Systems • Excellent interpersonal, oral, and written communication skills in English
• Mentoring and guidance offered • Collaborative and supportive work environment • Opportunity to work with diverse therapeutic areas
Apply Now🕒 March 13
Manage full clinical site monitoring services, ensuring project compliance and site data management. Role involves critical liaison functions and oversight of monitoring services.