
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.
🔥 10 minutes ago
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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.
• 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 • Ensure site compliance with IP receipt, accountability and return or destruction • Conduct accompanied site visits for assessment or training of other CRAs as requested and appropriate
• 5+ years of experience as a Clinical Research Associate • 4-year university degree or RN/BSN in Nursing • Experience with CNS and Early Phase/Healthy Volunteer studies is required • Willingness to travel • 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
• Cultivating a diverse and inclusive environment • Professional growth and success opportunities
Apply Now🕒 June 16
Senior Clinical Research Associate at Precision for Medicine conducting clinical research and ensuring site compliance with protocols and standards. Responsibilities include site management, monitoring, and reporting duties.
🕒 June 16
🕒 June 6
Manage and deliver clinical site monitoring services for diverse multinational projects. Act as primary liaison between CRAs and project team while ensuring regulatory compliance in Australia.
🗣️🇳🇱 Dutch Required