Provide comprehensive support to Pfizer Oncology’s Global Regulatory Strategy Teams (GRST) and Submission Teams
Develop and manage submission timelines and milestones using appropriate tools
Identify efficiencies to enable fast filings and convert submission timelines into clear, actionable tasks
Contribute to the design and implementation of processes that enhance workflow efficiency
Organize and manage GRST, Submission Team, MCI and other leadership pre-alignment meetings
Proactively identify and resolve project issues to meet productivity, quality, and organizational goals
Lead or co-lead projects, effectively managing time and resources for oneself
Develop and maintain templates, dashboards, team rosters, document reviewer lists, and action trackers
Independently prepare comprehensive status reports, timelines, tables, graphs, correspondence, and presentations as needed

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
Strong project management skills with demonstrated attention to detail
Proficiency in MS Word, Excel, PowerPoint, and Outlook; understanding of MS Project is preferred

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

Manager, Regulatory Program Management – Submission Strategy, Oncology

Key skills