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Director, Medical Information
DBV Technologies. Provide strategic leadership, development, and operational execution for the Medical Information function .
Posted 10/8/2026full-timeWarren • New Jersey • United StatesLead💰 $190,000 - $210,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in medical information strategy development and execution, with a strong focus on compliance with FDA regulations and PhRMA guidelines. Proven ability to analyze clinical data and communicate effectively with diverse audiences in the pharmaceutical or biotechnology industry.
Highest-signal resume keywords
Advanced Scientific DegreeMedical Information Strategy DevelopmentFDA Regulations ComplianceTechnical Writing SkillsImmunology Expertise
ATS Keywords
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Hard Skills
Medical Information ManagementClinical Trial AnalysisEvidence-Based Response DevelopmentData AnalysisProduct Launch Support
Soft Skills
Effective CommunicationLeadershipCollaboration
Industry Keywords
Pharmaceutical IndustryBiotechnology IndustryPhRMA GuidelinesIFPMA Codes of PracticeMedical Affairs
About the role
Key responsibilities & impact- Provide strategic leadership, development, and operational execution for the Medical Information function
- Ensure accurate, compliant, and timely communication of scientific and clinical information regarding DBV’s EPIT platform
- Develop and execute a comprehensive global medical information strategy supporting launch and lifecycle of the VIASKIN® Patch platform
- Oversee development of evidence-based responses for global inquiries
- Establish and manage infrastructure for intake, tracking, and reporting of medical inquiries
- Analyze medical information trends and provide actionable insights to Medical, Commercial, Clinical, and Regulatory stakeholders
- Supervise external medical information vendors
- Contribute to other Medical Affairs and company projects as needed
Requirements
What you’ll need- Advanced scientific degree (PharmD, PhD, or MD) is required
- Expertise in immunology, allergy, or pediatric medicine preferred
- Minimum of 5 years of experience in the pharmaceutical or biotechnology industry in a medical information position
- Proven track record of supporting a product through a launch phase is a significant plus
- Comprehensive understanding of FDA regulations governing the communication of medical and scientific data
- Advanced ability to analyze complex clinical trial results and translate them into concise, evidence-based responses
- Strict adherence to PhRMA guidelines and international codes of practice (e.g., IFPMA)
- Highly developed technical writing skills
- Ability to communicate effectively with diverse scientific and non-scientific audiences