Manager, Regulatory Program Management & Submission Strategy (oncology)

Pfizer

Multiple Locations
Base: $99,200.00 - $165,400.00; bonus/equity: 12.5...
Hybrid - must be onsite an average of 2.5 days per week.
Regulatory program management
Submission strategy
Oncology portfolio
Pfizer is seeking a Manager for Regulatory Program Management and Submission Strategy within its Oncology division to oversee regulatory activities and ensure compliance with timelines. The role emphasizes project management, collaboration with diverse teams, and effective communication with senior stakeholders

Job Summary

  • The Manager, RPMSS plays a critical role in partnering with regulatory strategists to advance regulatory and submission activities for assigned programs within the oncology portfolio.
  • Develop and manage submission timelines and milestones using appropriate tools, identifying efficiencies to enable fast filings and convert submission timelines into clear, actionable tasks with proactive follow-up to ensure on-time delivery.
  • The annual base salary for this position ranges from $99,200.00 to $165,400.00, with eligibility for participation in Pfizer’s Global Performance Plan with a bonus target of 12.5% of the base salary and eligibility to participate in our share based long term incentive program.

Matching Summary

Match Score: 85

Pfizer is seeking a Manager for Regulatory Program Management and Submission Strategy within its Oncology division to oversee regulatory activities and ensure compliance with timelines. The role emphasizes project management, collaboration with diverse teams, and effective communication with senior stakeholders.

Salary

Base: $99,200.00 - $165,400.00; Bonus/Equity: 12.5% bonus target; Benefits: Comprehensive and generous benefits

Skills & Requirements

Must-have

  • regulatory program management
  • submission strategy
  • oncology portfolio
  • regulatory timelines and commitments
  • cross-functional collaboration

Nice-to-have

  • high energy level
  • sense of urgency
  • creativity
  • decisiveness
  • work hard under pressure

Key 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
  • Experienced in managing day-to-day planning and project management
  • Experienced in communicating and interacting with senior executive stakeholders
  • Experienced in managing multiple, competing tasks simultaneously
  • Demonstrated ability to work collaboratively with diverse teams
  • Proficiency in MS Word, Excel, PowerPoint, and Outlook
  • Permanent work authorization in the United States

Work Rights

Permanent work authorization required

Tailored Resume

Cover Letter