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Director, Scientific Communications & Medical Education

Job in Berkeley Heights, Union County, New Jersey, 07922, USA
Listing for: BioNTech IMFS
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Healthcare Management, Healthcare Administration
Salary/Wage Range or Industry Benchmark: 125000 - 150000 USD Yearly USD 125000.00 150000.00 YEAR
Job Description & How to Apply Below

Director, Scientific Communications & Medical Education

New Jersey, US | full time | Job

Director, US-Scientific Communications and Medical Education Leadership – Driving Innovation in Oncology

Department: US Medical Affairs – Oncology

Reports to:

Executive Director, US Medical Affairs Operations

Position Summary:

BioNTech, a global leader in immunotherapy and medical innovation, is seeking a dynamic and visionary Director, US
- Scientific Communications and Medical Education Leadership to join our US Medical Affairs team. This role is pivotal in advancing BioNTech’s mission to transform lives through cutting‑edge science and patient‑focused solutions. Reporting to the Head of US-Medical Affairs Operations, this leadership role is instrumental in shaping and executing the strategic vision of scientific communication and medical education strategies to support the company’s U.S. medical affairs objectives while working closely with global teams to ensure alignment with overarching corporate goals.

As part of BioNTech’s mission to revolutionize healthcare, this position will lead the development and execution of scientific communication and medical education strategies, partnering across the organization for a fast‑growing business. This role will serve as a key liaison between U.S. and global stakeholders, ensuring the dissemination of accurate, impactful, and compliant scientific and medical information to healthcare professionals, patients, and other key audiences.

This is an opportunity to drive innovation, enhance operational excellence, and contribute to delivering transformative therapies to patients worldwide.

Scientific Communications:
  • Develop and execute a U.S.

    -specific scientific communications strategy in alignment with global objectives and regional needs.
  • Lead the creation, review, and dissemination of U.S.

    -focused scientific content, including publications, abstracts, posters, presentations.
  • Partner with global teams to adapt and localize global scientific platforms, such as disease‑state education materials and FAQs, for the U.S. market.
  • Ensure all U.S. scientific communications comply with FDA regulations, PhRMA guidelines, and other relevant standards.
  • Collaborate with U.S. commercial and marketing teams to ensure scientific accuracy and consistency in promotional materials.
  • Support medical information and review activities, ensuring alignment with compliance standards and scientific accuracy.
Medical

Education:

  • Design and implement U.S.

    -specific medical education programs, including CME, grants, and symposia, in collaboration with global teams.
  • Build and maintain relationships with U.S.

    -based Key Opinion Leaders (KOLs), healthcare professionals, and professional societies to support educational initiatives.
  • Partner with global teams to adapt and execute global medical education programs for U.S. audiences, ensuring regional relevance and compliance.
  • Manage U.S.

    -based external vendors and agencies to deliver high‑quality medical education programs.
  • Monitor and assess the effectiveness of U.S. medical education initiatives and provide feedback to cross‑functional teams for continuous improvement.
Cross‑Functional

Collaboration:

  • Serve as the primary U.S. point of contact for global scientific communications and medical education initiatives.
  • Collaborate with global medical affairs, clinical development, and commercial teams to ensure alignment of U.S. and global strategies.
  • Provide U.S. market insights to global teams to inform the development of scientific communication and education materials.
  • Contribute to global publication planning and ensure timely execution of U.S.

    -specific deliverables.
  • Participate in global medical affairs meetings and contribute to the development of global strategies and best practices.
Compliance and Quality Assurance:
  • Ensure all U.S. scientific communications and medical education activities comply with FDA regulations, PhRMA Code, ICMJE guidelines, and company policies.
  • Maintain high standards of scientific rigor, accuracy, and integrity in all deliverables.
  • Collaborate with legal, regulatory, and compliance teams to ensure all U.S. activities meet internal and external…
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