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.
Manage submission timelines and milestones
Develop and implement efficient processes
Track and analyze business metrics
Pfizer is seeking a Manager for Regulatory Program Management & Submission Strategy in oncology, responsible for overseeing regulatory activities and ensuring timely submissions. The role requires collaboration with cross-functional teams and effective project management skills in the biopharmaceutical industry

Job Summary

  • Provides comprehensive regulatory program management support to ensure alignment with and execution of Pfizer Oncology’s regulatory strategies and submission deliverables.
  • Develops and manages submission timelines and milestones, identifies efficiencies for fast filings, and ensures on-time delivery through proactive follow-up.
  • Offers a salary range of $99,200.00 to $165,400.00, eligibility for a bonus plan, and comprehensive benefits including a 401(k) plan.

Matching Summary

Match Score: 85

Pfizer is seeking a Manager for Regulatory Program Management & Submission Strategy in oncology, responsible for overseeing regulatory activities and ensuring timely submissions. The role requires collaboration with cross-functional teams and effective project management skills in the biopharmaceutical industry.

Salary

Base: $99,200.00 - $165,400.00; Bonus/Equity: 12.5% bonus target; Benefits: Comprehensive benefits package including 401(k)

Skills & Requirements

Must-have

  • Manage submission timelines and milestones
  • Develop and implement efficient processes
  • Track and analyze business metrics
  • Partner with regulatory strategists
  • Oncology portfolio regulatory strategy

Nice-to-have

  • High energy level and sense of urgency
  • Navigate fast-paced, highly matrixed environment
  • Respond with professionalism
  • Model Pfizer Values and Core Competencies

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
  • Experience managing day-to-day planning and project execution
  • Experience communicating with senior executive stakeholders
  • Experience managing multiple competing tasks
  • Demonstrated ability to work collaboratively with diverse teams
  • Proficiency in MS Word, Excel, PowerPoint, and Outlook
  • Understanding of MS Project is preferred

Work Rights

Permanent work authorization required

Tailored Resume

Cover Letter