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.
Senior Clinical Research Associate
🕒 April 16
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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
• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects • Involved in all stages of the clinical study, including identifying potential sites to participate • Perform various study start-up activities such as working with sites to collect appropriate regulatory documents • Support the negotiation of contracts and budgets • Train the sites to collect data properly and report any potential safety-related events • Manage the site's activities during study maintenance • Close down research activities at the sites once the study has concluded • Conduct study initiation visits (SIVs) while ensuring compliance with obtaining informed consent
🎯 Requirements
• 5+ years of experience as a Clinical Research Associate • 4-year university degree or RN/BSN in Nursing • Willingness to travel required • Excellent interpersonal, oral, and written communication skills in English • Superior organizational skills with attention to details • Ability to work with little or no supervision • Proficiency in Microsoft Office, CTMS and EDC Systems
🏖️ Benefits
• Equal employment opportunities to all employees and applicants • Committed to enabling professionals from all backgrounds and experiences to succeed • Prioritize attracting diverse talent and cultivating an inclusive environment
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