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.
Risk and Central Monitoring Manager
🕒 April 23
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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
• Coordinates cross-functional risk management and central monitoring activities for assigned clinical trials • Supports study teams by prioritizing quality across the study and ensuring consistency within programs, therapeutic areas, and/or sponsors • Oversees all Risk-Based Quality Management activities on assigned studies • Develops the Central Monitoring Plan for the assigned study and gains Global Project Lead (GPL) and sponsor approval • Delivers training to study teams regarding the RBQM strategy
🎯 Requirements
• Bachelor of Science (BSc), Registered Nurse (RN), or an equivalent combination of knowledge, skills, and experience • At least five years of experience in clinical research • At least three years of experience and knowledge in risk-based monitoring and associated International Council for Harmonisation and regulatory guidance • Prior experience in central monitoring and as a Risk Manager
🏖️ Benefits
• Competitive salary • Flexible working hours • Professional development opportunities • Health insurance • Paid time off
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