BioNTech SE
Director, Scientific Communications & Medical Education
BioNTech SE, Berkeley Heights, New Jersey, us, 07922
Director, Scientific Communications & Medical Education
New Jersey, US | full time | Job ID: 9691
Director, US-Scientific Communications and Medical Education Leadership – Driving Innovation in Oncology
Department: US Medical Affairs – Oncology
Location: Berkeley Heights, NJ (Hybrid)
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 of US Scientific Communications and Medical Education 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. The Director will spearhead the strategic vision of scientific communication and medical education strategies, supporting the company’s U.S. medical affairs objectives while working closely with global teams to ensure alignment with corporate goals.
Key Responsibilities
Develop and execute a U.S.-specific scientific communications strategy aligned with global objectives and regional needs.
Lead the creation, review, and dissemination of U.S.-focused scientific content, including publications, abstracts, posters, and 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.
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.
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.
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 standards.
Establish and monitor key performance indicators to measure the impact of educational events and provide actionable insights and data‑driven recommendations to executive leadership.
Inspire, mentor, and empower a high‑performing, matrixed team responsible for tactical execution and define clear roles and responsibilities while cultivating a culture of excellence and innovation.
Foster collaboration, remove barriers to efficiency, and drive accountability across stakeholders.
Qualifications
Advanced scientific or healthcare degree (PharmD, PhD, MD, or equivalent strongly preferred).
Minimum of 8 years of experience in scientific communications or medical education within the pharmaceutical, biotechnology, or 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, with a focus on advancing scientific excellence and patient‑centric solutions.
Proven 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 (e.g., FDA, OPDP) and industry standards (e.g., 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 accommodate moderate travel (~25%) depending on specific project demands and organizational requirements.
Key Competencies
Strategic Vision: Ability to set a compelling vision and translate it into actionable plans that drive impact.
Leadership: Inspires, empowers, and develops teams to achieve shared goals.
Process Excellence: Passion for designing and optimizing processes in highly regulated environments.
Collaboration: Collaborate with Compliance, Legal, and Regulatory teams to ensure all activities uphold BioNTech’s commitment to ethical standards, transparency, and regulatory excellence.
Analytical Rigor: Data‑driven decision‑maker with a focus on quality, accuracy, and compliance.
Expected Pay Range $210,000/year to $257,000/year + benefits, annual bonus & equity (bonus and equity are variable and dependent on company and individual performance).
Your Benefits
Medical, Dental and Vision Insurance
Life, AD&D, Critical Illness Insurance
Pre‑tax HSA & FSA, DCRA Spending Accounts
Employee Assistance & Concierge Program (EAP) available 24/7
Parental and Childbirth Leave & Family Planning Assistance
Sitterstream: Virtual Tutoring & Childcare Membership
Paid Time Off: Vacation, Sick, Bereavement, Holidays (including Floating) & Year‑End U.S. Shutdown
401(K) Plan with Company Match
Tuition Reimbursement & Student Loan Assistance Programs
Wellbeing Incentive Platforms & Incentives
Professional Development Programs
Commuting Allowance and subsidized parking
Discounted Home, Auto & Pet Insurance
…and more! More details to be shared.
Apply Now We look forward to your application! Apply for our New Jersey, US location and simply send us your documents using our online form.
By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider “HireRight”. You will be informed accordingly by your BioNTech recruiter.
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Director, US-Scientific Communications and Medical Education Leadership – Driving Innovation in Oncology
Department: US Medical Affairs – Oncology
Location: Berkeley Heights, NJ (Hybrid)
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 of US Scientific Communications and Medical Education 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. The Director will spearhead the strategic vision of scientific communication and medical education strategies, supporting the company’s U.S. medical affairs objectives while working closely with global teams to ensure alignment with corporate goals.
Key Responsibilities
Develop and execute a U.S.-specific scientific communications strategy aligned with global objectives and regional needs.
Lead the creation, review, and dissemination of U.S.-focused scientific content, including publications, abstracts, posters, and 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.
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.
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.
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 standards.
Establish and monitor key performance indicators to measure the impact of educational events and provide actionable insights and data‑driven recommendations to executive leadership.
Inspire, mentor, and empower a high‑performing, matrixed team responsible for tactical execution and define clear roles and responsibilities while cultivating a culture of excellence and innovation.
Foster collaboration, remove barriers to efficiency, and drive accountability across stakeholders.
Qualifications
Advanced scientific or healthcare degree (PharmD, PhD, MD, or equivalent strongly preferred).
Minimum of 8 years of experience in scientific communications or medical education within the pharmaceutical, biotechnology, or 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, with a focus on advancing scientific excellence and patient‑centric solutions.
Proven 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 (e.g., FDA, OPDP) and industry standards (e.g., 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 accommodate moderate travel (~25%) depending on specific project demands and organizational requirements.
Key Competencies
Strategic Vision: Ability to set a compelling vision and translate it into actionable plans that drive impact.
Leadership: Inspires, empowers, and develops teams to achieve shared goals.
Process Excellence: Passion for designing and optimizing processes in highly regulated environments.
Collaboration: Collaborate with Compliance, Legal, and Regulatory teams to ensure all activities uphold BioNTech’s commitment to ethical standards, transparency, and regulatory excellence.
Analytical Rigor: Data‑driven decision‑maker with a focus on quality, accuracy, and compliance.
Expected Pay Range $210,000/year to $257,000/year + benefits, annual bonus & equity (bonus and equity are variable and dependent on company and individual performance).
Your Benefits
Medical, Dental and Vision Insurance
Life, AD&D, Critical Illness Insurance
Pre‑tax HSA & FSA, DCRA Spending Accounts
Employee Assistance & Concierge Program (EAP) available 24/7
Parental and Childbirth Leave & Family Planning Assistance
Sitterstream: Virtual Tutoring & Childcare Membership
Paid Time Off: Vacation, Sick, Bereavement, Holidays (including Floating) & Year‑End U.S. Shutdown
401(K) Plan with Company Match
Tuition Reimbursement & Student Loan Assistance Programs
Wellbeing Incentive Platforms & Incentives
Professional Development Programs
Commuting Allowance and subsidized parking
Discounted Home, Auto & Pet Insurance
…and more! More details to be shared.
Apply Now We look forward to your application! Apply for our New Jersey, US location and simply send us your documents using our online form.
By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider “HireRight”. You will be informed accordingly by your BioNTech recruiter.
#J-18808-Ljbffr