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Director, Medical Review

DBV Technologies
Full-time
On-site
Trenton, New Jersey, United States
Director, Medical Review
DBV Technologies is a global clinical stage biopharmaceutical company on a mission to develop treatment options for food allergies and immunologic diseases with significant unmet medical need using our innovative epicutaneous immunotherapy technology platform, Viaskin® Patch. The Director, Medical Review plays a key role within the Medical Affairs organization and is responsible for ensuring medical and scientific accuracy of promotional and non‑promotional materials in compliance with US and other health agency laws and regulations. This role supports both promotional and medical materials through the Promotional Review Committee (PRC) and the Medical Review Committee (MRC), working closely with Medical Affairs, Regulatory, Legal/Compliance, and Marketing.

Location: Warren, New Jersey (on site 3 days a week / remote 2 days a week)

Salary Range: 165‑200K

Key Responsibilities

Lead the Medical Review process of medical and promotional materials in partnership with internal stakeholders, including medical slides, training materials, and advertising content.

Provide medical and scientific review of promotional and non‑promotional materials to verify data accuracy, proper substantiation, and consistency with clinical study reports, clinical guidance, and scientific literature.

Work closely with Medical Affairs Communications Leadership to ensure external communications meet regulatory and scientific expectations and align with medical and brand strategy.

Collaborate with material owners and reviewers to clarify data interpretation and ensure alignment across assigned therapeutic areas.

Participate in review meetings providing medical input on disease education, product communications, pipeline materials, training documents, and more.

Ensure standardization of defined policies, SOPs, and best practices, and provide feedback and recommendations to optimize these processes and workflows.

Partner and collaborate with Medical Affairs colleagues and key internal partners including Regulatory, Legal, Compliance, Marketing, and Commercial teams.

Represent Medical Affairs in functional and operational meetings related to the Promotional or Medical Review Process and Best Practices.

Participate in training programs for internal stakeholders to ensure best practices, up‑to‑date knowledge, and operational excellence.

Support Medical Affairs with additional projects, as needed.

Qualifications

Doctoral degree in a health science related field (MD, PhD, PharmD, DO) preferred.

Minimum 8‑10 years of relevant experience in the medical review of scientific and promotional material in a pharmaceutical or biotech setting.

Working knowledge of US, EU, and Canadian health agency regulatory standards.

Well‑versed in scientific and clinical trial knowledge, documents, and vocabulary.

Proficiency in Microsoft Office applications required; knowledge of Veeva systems desirable.

Highly collaborative, exceptional attention to detail, values scientific accuracy, and demonstrates excellent organizational skills.

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.

DBV Technologies was founded by pediatricians who believed that food allergies could one day be treated safely and effectively. We are advancing epicutaneous immunotherapy using the Viaskin™ platform to develop treatment options for patients with food allergies and other immunologic diseases.

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