Manager, Regulatory Program Management – Submission Strategy (Oncology)

Role Overview

• Provide comprehensive regulatory program management support
• Ensure alignment with and execution of Pfizer Oncology’s regulatory strategies
• Coordinate and prioritize regulatory activities
• Facilitate decision-making processes
• Oversee information flow to ensure adherence to regulatory timelines
• Partner with regulatory strategists to advance regulatory and submission activities

Requirements

• Bachelor’s Degree with 4+ years of experience or Master’s Degree with 2+ years of experience
• 2-4+ years of experience in the biopharmaceutical industry – understanding of Oncology preferred
• Experienced in managing day-to-day planning and project management to enable execution of complex strategies
• Experienced in communicating and interacting with senior executive stakeholders
• Experienced in managing multiple, competing tasks simultaneously
• Demonstrated ability to work collaboratively with diverse teams and manage a team of cross-functional colleagues
• Demonstrated understanding of systems and structures, and ability to implement efficient processes
• Proficiency in MS Word, Excel, PowerPoint, and Outlook; understanding of MS Project is preferred

Benefits

• 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
• Paid vacation
• Holiday and personal days
• Paid caregiver/parental and medical leave
• Health benefits to include medical, prescription drug, dental and vision coverage