Director, Medical Information

DBV Technologies; Virginia; In loco; USD 190.000 - 210.000; Tempo pieno

Descrizione del lavoro

DBV Technologies seeks a Director of Medical Information to lead strategic and operational Medical Information activities for the EPIT platform, ensuring accurate, compliant medical knowledge is communicated to healthcare professionals, patients, and external stakeholders.

Based in Warren, New Jersey with 3+ on-site days, the role leads global medical information strategy, develops evidence-based responses, oversees data intake and reporting, and partners with Medical, Commercial, Clinical and

Competenze

• 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 and the ability to communicate effectively with diverse scientific and non-scientific audiences.

Mansioni

• Develop and execute a comprehensive global medical information strategy to support launch and lifecycle of the VIASKIN® Patch platform
• Oversee the development of high-quality, evidence-based responses for global inquiries
• Establish and manage the infrastructure for intake, tracking, and reporting of medical inquiries, ensuring timely and compliant delivery of information
• Analyze medical information trends to provide actionable insights to Internal Stakeholders (Medical, Commercial, Clinical, and Regulatory teams)
• Supervise external medical information vendors to ensure operational excellence and adherence to DBV’s quality standards
• Contribute to other Medical Affairs and company projects, as needed

Formazione

PharmD, PhD, or MD

Descrizione del lavoro

Description:

The Director of Medical Information is responsible for the strategic leadership, development, and operational execution of the Medical Information function at DBV Technologies. This role ensures the accurate, compliant, and timely communication of scientific and clinical information regarding DBV’s epicutaneous immunotherapy (EPIT) platform to healthcare professionals, patients, and other external stakeholders. The Director serves as the primary subject matter expert for the dissemination of medical knowledge and ensures all activities comply with global regulatory standards.

Location:Warren, New Jersey - 3 + days on site

Salary Range:190-210K

Key Responsibilities:

• Develop and execute a comprehensive global medical information strategy to support launch and lifecycle of the VIASKIN® Patch platform

• Oversee the development of high-quality, evidence-based responses for global inquiries

• Establish and manage the infrastructure for intake, tracking, and reporting of medical inquiries, ensuring timely and compliant delivery of information

• Analyze medical information trends to provide actionable insights to Internal Stakeholders (Medical, Commercial, Clinical, and Regulatory teams)

• Supervise external medical information vendors to ensure operational excellence and adherence to DBV’s quality standards

• Contribute to other Medical Affairs and company projects, as needed
  

Qualifications:

• 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 and the ability to communicate effectively with diverse scientific and non-scientific audiences

Behavioral skills:

• Curiosity: Keep on exploring uncharted territories. Always ask "why?" and more importantly "why not?",

• Courage: Take smart risks, mentor each other to always do better & be accountable for our choices, our opinions, and our actions,

• Collaboration: Teamwork and spirit. Support each other and be equally involved in the achievement of our common goals,

• Credibility: Be transparent, follow through and build trust. Educate ourselves about our unique technology.