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Director, Scientific Communications & Medical Education

BioNTech SE
Full-time
Remote friendly (Berkeley Heights, NJ)
United States
Medical Affairs

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Role Summary

Director, US-Scientific Communications and Medical Education Leadership – Driving Innovation in Oncology. Location: Berkeley Heights, NJ (Hybrid). Reports to: Executive Director, US Medical Affairs Operations.

Responsibilities

  • 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 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.

Qualifications

  • Advanced scientific or healthcare degree (PharmD, PhD, MD, or equivalent strongly preferred).
  • Minimum of 8 years of experience in scientific communications, medical education within the pharmaceutical/biotechnology/healthcare industry, with at least 5 years in an oncology medical affairs role.
  • Demonstrated success in leading the development and execution of oncology scientific communication and medical education strategies.
  • Experience working in a global organization and collaborating with cross-functional, international teams.
  • Strong understanding of compliance and regulatory frameworks governing scientific exchange.
  • Deep understanding of U.S. regulatory requirements (FDA, OPDP) and industry standards (GPP, ICMJE, PhRMA Code).
  • Exceptional communication, negotiation, and stakeholder management skills.
  • Ability to manage multiple projects and priorities in a fast-paced, matrixed environment.
  • Ability to travel moderately (~25%) to conferences, internal meetings, field visits, and partnerships.

Skills

  • Strategic Vision: translate vision into actionable plans.
  • Leadership: develop and empower teams.
  • Process Excellence: design and optimize regulated processes.
  • Collaboration: work with Compliance, Legal, Regulatory teams to maintain ethical standards and regulatory excellence.
  • Analytical Rigor: data-driven with emphasis on quality and compliance.

Education

  • Advanced scientific or healthcare degree (PharmD, PhD, MD, or equivalent strongly preferred).