Worldwide Clinical Trials
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.
1001 - 5000 employees
🧬 Biotechnology
đź’Š Pharmaceuticals
⚕️ Healthcare Insurance
Senior Auditor, Audits and Inspections Program
November 5
Worldwide Clinical Trials
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.
1001 - 5000 employees
🧬 Biotechnology
đź’Š Pharmaceuticals
⚕️ Healthcare Insurance
đź“‹ Description
• Champions and adheres to Worldwide’s Quality Management System (QMS) • Serves as a positive ambassador of the QA organization with internal and external customers • Develops and executes to personal and QA goals and objectives • Hosts external audits and regulatory inspections • Ensures quality deliverables, on time, and in compliance with regulations and Worldwide processes • Oversees, monitors and reports on QA audits
🎯 Requirements
• M.S. in a scientific or allied health field • 5+ years of relevant GCP, GcLP, GLP, GVP, and / or GPP experience • Excellent understanding of the Drug Development Process • Minimum 3 years of Quality Assurance auditing experience • IT literate with Microsoft based applications proficiency
🏖️ Benefits
• Supportive teams • Training material and/or delivers training • Diverse and inclusive environment
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