Senior Medical Director, Medical Affairs

🔥 12 hours ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $175k - $348k / year

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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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

• Medically manage assigned clinical trials as Medical Monitor • Serve as Global Lead Medical Monitor for pan-regional and/or global trials • Collaborate with Medical & Safety project team members to process Serious Adverse Events • Provide therapeutic and protocol-specific training to project teams • Contribute medical input to clinical development programs, study protocols, research papers, and client-focused white papers • Provide after-hours medical support for assigned projects • Support Business Development through proposal generation, feasibility assessments, proposal/contract review, and sponsor meetings • Review or assist with final study reports and other study documentation • Maintain competence in assigned projects, therapeutic advances, and marketplace developments • Interact with other functional areas to ensure successful project execution and client satisfaction • Identify, document, and resolve out-of-scope work • Assist with departmental revenue targets and other senior-management-directed activities • Maintain compliance with ethical, legal, and regulatory standards • Mentor other medical staff and support department and company leadership • Maintain clinical and therapeutic acumen through scholarly programs and lectures • Perform SAE-related medical review in the electronic safety database • Perform other duties as assigned

🎯 Requirements

• Medical Degree from an accredited institution of Medical Education • 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 • Excellent computer skills (Word, Excel, Access) • Excellent spoken and written English skills • Excellent organizational and time management skills • Excellent communication skills • Excellent presentation skills • Working knowledge of GCPs and regulatory requirements relating to clinical development and safety • Competence with SAE-related medical review in WORLDWIDE's electronic safety database

🏖️ Benefits

• Competitive benefits package depending on location • Transparent compensation and pay equity • Opportunity to work in an inclusive and equitable workplace