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
🔥 0 minutes ago
🐊 Florida – Remote
💵 $134.5k - $267.5k / year
⏰ Full Time
🔴 Lead
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
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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
• Medically manages clinical trials to which s/he is assigned as MM • Serves as Global Lead MM (GLMM) for pan-regional and/or global trial(s) • Collaborates with the other members of the Medical & Safety project teams to process Serious Adverse Events (SAEs) • Provides therapeutic and protocol-specific training to the project teams • Contributes medical input into the design of clinical development programs
🎯 Requirements
• Medical Degree from an accredited institution of Medical Education • At least 2 years of medical monitoring in clinical research or related industry • Valid passport and ability to travel as required
🏖️ Benefits
• Competitive benefits package depending on location • Health insurance • Paid time off • Flexible environment
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