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Senior Associate, Early Phase Oncology Regulatory Specialist

1 mese fa

Milano, Lombardia, Italia Pfizer A tempo pieno
Job Summary

Pfizer is seeking a highly skilled Senior Associate to join our Early Phase Oncology Regulatory team. As a key member of our team, you will be responsible for representing the EU region in regulatory matters related to our early-stage oncology portfolio.

Key Responsibilities
  • Provide regional strategic expertise as a member of the Global Regulatory Strategic Team (GRST)
  • Lead and implement EU regulatory strategies in agreement with key stakeholders for assigned projects/products and in line with the company goals
  • Accountable for timely submissions and approvals in the EU region
  • Accountable for ensuring optimal regulatory interactions with Health Authorities, in relation to the designated early-stage oncology portfolio within the EU
Qualifications
  • Scientific Degree. A higher degree may be an advantage but is not essential
  • Proven experience in managing national and/or EU regulatory process and registration aspects of the drug development process particularly clinical trials experience at least in one country
  • Previous experience as a national and/or EU regulatory liaison for at least one product in different therapeutic areas and in different stages of the product life cycle is highly desirable
About Pfizer

Pfizer is a patient-centric company guided by our four values: courage, joy, equity, and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives. We are committed to creating a trusting, flexible workplace culture which encourages employees to achieve work-life harmony, attracts talent, and enables everyone to be their best working self.

We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating diversity in all its forms – allowing us to be as diverse as the patients and communities we serve.