Pfizer – Director, Global Regulatory Sciences – Vaccines
Location Options:
Cambridge, Massachusetts
Pearl River, New York
Collegeville, Pennsylvania
New York City, New York
Employment Type: Full-time
Job ID: 4940082
Posted: 15 Days Ago
As the Director of Global Regulatory Sciences – Vaccines, you will serve as the Global Regulatory Lead and U.S. Regional Regulatory Lead for Pfizer's combination Influenza/COVID-19 mRNA vaccine program, as well as the U.S. Regional Regulatory Lead for the COVID-19 mRNA vaccine program. Your primary responsibility will be to develop and execute global and U.S. regulatory strategies, ensuring compliance with applicable regulations and facilitating timely access to life-saving treatments.
Regulatory Strategy Development: Lead the creation, updating, and communication of global regulatory strategies for assigned vaccine projects/products, including mechanisms of action and/or indications.
Cross-Functional Collaboration: Act as a key member of project/product teams, partnering with leaders to ensure the delivery of project/product goals aligned with the endorsed Global Regulatory Strategy.
Regulatory Agency Interaction: Represent Pfizer in interactions with health authorities, ensuring appropriate communication and representation for assigned projects/products.
Mentorship and Development: Mentor and develop regulatory professionals, fostering a collaborative environment to meet project/product objectives.
Stakeholder Engagement: Cultivate strong relationships with regulators, professional bodies, external experts, opinion leaders, and internal stakeholders to support regulatory activities.
Governance Participation: Engage in governance committees as necessary, ensuring alignment with strategic goals and regulatory requirements.
Minimum Requirements:
Education: Bachelor’s degree required; Master’s, PharmD, or PhD preferred.
Experience: Minimum of 8 years in clinical regulatory affairs, with a focus on vaccines.
Skills:
Deep understanding of drug development and license maintenance processes.
Proficiency in regulatory codes, guidance, and technologies.
Experience with systems and electronic technologies supporting regulatory activities.
Proficiency in Microsoft Office.
Excellent communication skills.
Preferred Attributes:
Ability to navigate ambiguity and facilitate discussions to uncover optimal solutions.
Strong collaborative orientation with service provider and business partner focus.
Experience leading teams within a matrix structure.
Proven track record in fostering a culture of innovation and continuous improvement.
Strategic thinking and problem-solving capabilities.
Adaptability to regulatory changes while maintaining high standards.
Base Salary: $169,700 – $282,900 annually.
Bonus: Eligible for Pfizer’s Global Performance Plan with a target bonus of 20% of base salary.
Long-Term Incentives: Participation in share-based long-term incentive programs.
Retirement Plans: 401(k) plan with Pfizer Matching Contributions and additional Pfizer Retirement Savings Contribution.
Paid Time Off: Paid vacation, holiday, and personal days; paid caregiver/parental and medical leave.
Health Benefits: Comprehensive medical, prescription drug, dental, and vision coverage.
Note: Compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Work Location Assignment: Hybrid/site-based, requiring an average of 2.5 days per week on-site.
Travel Requirements: Limited travel.
Relocation Assistance: May be available based on business needs and/or eligibility.
Equal Opportunity Employer: Pfizer is committed to equal opportunity in employment and complies with all applicable laws governing nondiscrimination and work authorization requirements.
For more details and to apply, visit the Pfizer Careers Page.
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