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.
Medical Director, Medical Affairs – Neurology
🕒 April 24
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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
• Serves as Global Lead Medical Monitor (GLMM) for pan-regional and/or global trial(s) • Provides therapeutic and protocol-specific training to project teams • Contributes medical input into the design of clinical development programs • Maintains a high level of competence with assigned projects • Assists in the annual attainment of departmental revenue targets
🎯 Requirements
• Medical Degree from an accredited institution of Medical Education • Neurology Board Certification • 6-8 years in the CRO, Pharma or Biotech industry with the medical monitoring or study physician role • Valid passport and ability to travel if required
🏖️ Benefits
• Diverse and inclusive environment • Personal development opportunities • Hands-on, accessible leaders
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