Worldwide Clinical Trials
1001 - 5000 employees
🧬 Biotechnology
đź’Š 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
đź•’ April 29
🇬🇧 United Kingdom – Remote
⏰ Full Time
đźź Senior
🔬 Research Analyst
🇬🇧 UK Skilled Worker Visa Sponsor
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Worldwide Clinical Trials
1001 - 5000 employees
🧬 Biotechnology
đź’Š 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.
đź“‹ Description
• Responsible for site qualification, initiation, interim monitoring, site management, and study close-out visits. • Provide mentoring and guidance to less experienced CRAs and site staff when needed. • Document site visit findings via written reports. • Assess, monitor, and train study site staff on protocol adherence as required. • Review study subject safety information and informed consent. • Conduct source document verification for compliance, patient safety, and veracity of data. • Review CRFs using paper or electronic data capture systems and assist sites with data query resolution. • Provide applicable updates for site related documentation for filing in the Trial Master File (TMF).
🎯 Requirements
• 2+ years of experience as a Clinical Research Associate • 4-year university degree or RN/BSN in Nursing • Experience in Oncology and Neurology is required • Willingness to travel required
🏖️ Benefits
• Diverse and inclusive environment • Hands-on, accessible leaders • Supportive teams
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