Worldwide Clinical Trials
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.
Senior Clinical Trial Liaison – Oncology
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🔥 1 minute ago
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Worldwide Clinical Trials
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.
📋 Description
• Establish and maintain relationships with key opinion leaders, clinical sites, and site staff • Conduct targeted conversations with investigators and site staff about operational challenges, including patient recruitment and retention • Discuss clinical and scientific topics with investigators to ensure study endpoint quality, protocol understanding, study feasibility, and enrollment and retention of appropriate participants • Convey KOL and site staff feedback and insights to internal and external teams • Support and guide project teams with site identification and selection based on site capabilities and anticipated protocol challenges • Support business development activities through engagement with existing and prospective clients • Provide scientific and operational input on proposals in development • Attend and present at bid defense meetings
🎯 Requirements
• Doctoral degree required • Minimum 5 years’ experience in clinical research in academia, Pharma, Biotech, or CRO • Background in operational aspects of clinical research • Minimum 3 years’ experience in the assigned therapeutic area/indication • Demonstrated experience working directly with clinical sites and investigators • Strong background and experience in oncology studies • Excellent networking skills • Excellent written and verbal communication skills, with ability to interact with physicians and all levels of internal and external management • Excellent negotiation, influencing, and problem-solving skills • Self-motivated with proactive issue monitoring and management, including risk assessment and contingency planning • Combination of critical thinking, operational expertise, and efficiency
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