Director Medical Information

📋 Description

• Build and scale the MI function, focusing on US launch readiness.
• Oversee MI content: letters, FAQs, templates, AMCP dossiers.
• Lead vendor/center partnerships: training, KPIs, quality, budgets.
• Ensure scientifically accurate, compliant, evidence-based responses.
• Represent MI in MLR reviews and cross-functional forums.
• Monitor inquiries and insights to inform Medical Affairs strategy.

🎯 Requirements

• Advanced scientific or clinical degree (e.g., pharmD, PhD)
• 5+ years in biotech/pharma with MI/Medical Affairs experience
• Direct experience leading MI strategy, content, inquiry management, vendor oversight
• Strong understanding of regulatory, compliance, pharmacovigilance, and product complaints
• Excellent written and verbal communication; ability to deliver evidence-based responses
• Proficiency with MI systems and tools: Veeva Vault/CRM, MS Office, Adobe Acrobat

🎁 Benefits

• Remote work opportunities within the United States
• Travel to Cambridge, MA several times a year
• Supportive remote setup with reliable internet and video conferencing
• Accommodations available during the selection process