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Strategy Director, Global Regulatory Affairs

Meet North Carolina, United States

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Max Trafford

Max Trafford

Senior Recruitment Consultant

Client Overview:

Our client, a leading player in the pharmaceutical industry, is renowned for its collaborative and transparent environment. Unlike many large pharmaceutical companies, they offer direct visibility and interaction with high-level executives, providing a unique opportunity for professionals to have their expertise recognized and valued.


Position Summary:

The client is seeking a highly experienced professional to lead their regulatory strategy for a late-phase oncology program. This role offers the chance to shape the future of oncology treatments within a company that values innovation and strategic thinking. This position involves a critical alliance with major industry players such as Merck and AstraZeneca, and there are two openings depending on the candidate's background and skillset.


Key Responsibilities:

  • Spearhead regulatory submissions for the oncology portfolio, driving strategy with precision and expertise.
  • Focus on later-phase programs with opportunities to contribute to early-phase studies depending on pipeline needs.
  • Ensure strategic insights are heard and valued through direct reporting lines to VP level.


Candidate Requirements:

  • Minimum of 10 years in the pharmaceutical industry, with at least 7 years dedicated to global regulatory leadership roles.
  • Proven track record in leading regulatory strategies through successful oncology submissions.
  • Currently holding a Director Global Regulatory Lead (GRL) position, not seeking those looking to step up from Associate Director.
  • Demonstrated ability to drive high-level regulatory strategy and navigate complex regulatory landscapes.
  • Global experience and leading strategy in oncology are essential.


Compensation:

  • Base Salary + Bonus + Equity
  • Relocation Package: Comprehensive relocation assistance for exceptional candidates from different US time zones (MST or PST).


Why This Opportunity?

  • Work on cutting-edge oncology programs with a company that values strategic input.
  • Direct access to high-level leadership, ensuring your voice is heard.
  • A robust salary and benefits package that rewards expertise and contributions.


This is a rare opportunity to elevate your regulatory strategy career to the next level. Qualified candidates are encouraged to apply and help transform the future of oncology treatments.


Apply Now

  • Seniority level

    Director
  • Employment type

    Full-time
  • Job function

    Consulting, Project Management, and Research
  • Industries

    Research Services, Biotechnology Research, and Pharmaceutical Manufacturing

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