Medical Director, Medical Affairs – Neurology

🔥 1 minute ago

🌵 Arizona, California, +2 more states – Remote

🌵 Arizona – Remote 🏄 California – Remote 🎰 Nevada – Remote ☕ Washington – Remote

💵 $134.5k - $267.5k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

🦅 H1B Visa Sponsor

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

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

• Provide medical oversight and serve as the assigned Medical Monitor for clinical research studies. • Lead global and pan-regional trials as a Global Lead Medical Monitor. • Review and support the medical management of serious adverse events with Medical & Safety teams. • Deliver protocol-specific and therapeutic area training to project teams. • Contribute clinical and scientific expertise to study protocols, clinical development programs, research publications, and medical deliverables. • Support sponsor engagement and business development activities, including feasibility assessments, proposal development, and client meetings. • Review and contribute to clinical study reports and key study documentation. • Partner with cross-functional teams to ensure project delivery, regulatory compliance, and client satisfaction. • Mentor and support medical colleagues.

🎯 Requirements

• Medical Degree from an accredited institution of medical education. • At least 2 years of medical monitoring experience within clinical research or a related industry. • Strong knowledge of GCP, clinical development, safety processes, and applicable regulatory requirements. • Experience reviewing safety data and supporting serious adverse event assessment and management. • Excellent written and verbal communication, presentation, organizational, and time management skills. • Strong computer proficiency, including Microsoft Word, Excel, and Access. • Proficiency in English. • Valid passport and ability to travel as required.

🏖️ Benefits

• Competitive benefits package depending on location • Inclusive and equitable workplace • Transparent compensation and pay equity