
1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
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.
🔥 0 minutes ago
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1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
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.
• Conduct site qualification, initiation, interim monitoring, site management, and study close-out visits • Mentor and guide less experienced CRAs and site staff when needed • Document site visit findings through written reports • Assess, monitor, and train study site staff on protocol adherence • Review study subject safety information and informed consent • Conduct source document verification for compliance, patient safety, and data veracity • Review CRFs using paper or electronic data capture systems • Assist sites with data query resolution • Provide updates to site-related documentation for filing in the Trial Master File • Ensure site compliance with investigational product receipt, accountability, and return or destruction • Conduct accompanied site visits for assessment or training of other CRAs when requested and appropriate
• Excellent interpersonal, oral, and written communication skills in English • Superior organizational skills with attention to detail • Ability to work with little or no supervision • Proficiency in Microsoft Office, CTMS, and EDC systems • 5+ years of experience as a Clinical Research Associate • 4-year university degree or RN/BSN in Nursing • Willingness to travel • Oncology, CNS, or Rare Disease experience
• Diverse and inclusive work environment • Supportive and cohesive teams • Accessible, hands-on leadership • Opportunities for professional growth and development • Remote work arrangement
Apply Now🕒 2 days ago
Clinical research associate monitoring Phase 2/3 pharmaceutical trials for Ergomed, a specialist clinical research organization. Supporting sites, investigators, staff training, and regulatory submissions across the UK, France, and Belgium.
🗣️🇫🇷 French Required
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🇬🇧 United Kingdom – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟠 Senior
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🇬🇧 UK Skilled Worker Visa Sponsor
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🇬🇧 United Kingdom – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research
🇬🇧 UK Skilled Worker Visa Sponsor
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