Regulatory Strategist for Early Phase Oncology
1 settimana fa
Job Summary
As a Regulatory Strategist for Early Phase Oncology at Pfizer, you will be responsible for representing the EU region in regulatory sciences, providing regional strategic expertise, and leading EU regulatory strategies.
Key Responsibilities
- Represent the EU region in regulatory sciences, providing 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.
Required Skills
- 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.
Why Pfizer?
We are 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 aim to create 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.
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