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Senior Associate, Global Regulatory Strategy for Oncology

Pfizer
Full-time
Remote friendly (New London County, CT)
United States
$77,100 - $128,500 USD yearly
Corporate Functions

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Role Summary

In this role, you will:

  • Provide strategic product direction and interact with regulatory agencies to expedite the approval of pending registrations
  • Serve as the regulatory liaison throughout the product lifecycle, representing regulatory interests to marketing, research project teams, and government agencies
  • Develop and submit product registrations, progress reports, supplements, amendments, and periodic experience reports
  • Guide operational teams in managing projects, preparing resource forecasts, and identifying areas for improvement in products, processes, or services
  • Lead or co-lead moderately complex projects, managing time and resources effectively, and provide guidance to teams
  • Apply skills and discipline knowledge to contribute to departmental work and make decisions to resolve moderately complex problems
  • Work independently, receive instruction on unusual or complex problems, and determine objectives of assignments
  • Review own work, seek directional review from others, and mentor colleagues by reviewing their work
  • Collaborate with Global Chemistry Manufacturing and Controls and other key stakeholders to ensure well-defined and executed filing strategies for initial registrations and lifecycle submissions
  • Enhance efficiencies in regulatory submissions and processes by working across the organization with various stakeholders

Qualifications

  • Bachelors degree with at least 2 years of experience
  • Effective delivery in a complex matrix environment
  • Regulatory experience, including knowledge of New Drug Application (NDA) and Investigational New Drug (IND) submission processes
  • In-depth understanding of national and regional regulatory legislation and guidelines
  • Proficiency in pharmaceutical analytics technology, pharmacology, toxicology, and medicine
  • Leadership qualities and management skills
  • Strong written and verbal communication and interpersonal skills

Preferred Qualifications

  • Master's degree is highly desirable, coupled with relevant experience in the pharmaceutical industry
  • Background in pharmaceuticals, providing a solid foundation for the role
  • Experience in the pharmaceutical sector, enhancing the ability to contribute effectively
  • Advanced education and practical experience, ensuring a well-rounded and capable professional

Additional Details

  • Last date to apply is November 13, 2025
Apply now
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