Strategy Director, Global Regulatory Affairs

Meet
NC, United States
Full-time

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

24 days ago
Related jobs
Promoted
Meet
NC, United States

Support the lead regulatory strategy for late-phase oncology programs, ensuring alignment with global regulatory requirements. The client is seeking a seasoned professional to lead their regulatory strategy for a late-phase oncology program. Minimum of 8 years of industry experience, with at least 4...

Promoted
Verona Pharma
Raleigh, North Carolina

Verona Pharma is currently recruiting a Senior Director, Regulatory Affairs to join our team, reporting to our Senior Vice President, Regulatory Affairs. In the role of Senior Director, Regulatory Affairs, you will be responsible for overseeing and directing regulatory activities for new and mature ...

Promoted
Meet
NC, United States

Demonstrated ability to drive high-level regulatory strategy and navigate complex regulatory landscapes. The client is seeking a seasoned professional to lead their regulatory strategy for a late-phase oncology program. Spearhead regulatory submissions for the oncology portfolio, driving strategy wi...

Asahi Kasei Plastics North America
Cary, North Carolina

Implements and executes Veloxis’s global Regulatory strategy. Understanding of strategic and tactical role and deliverables of global Regulatory strategy in the drug and device development and commercialization process. Experience with communicating the Regulatory strategy, issues, and risks in writ...

Asahi Kasei America Inc
Cary, North Carolina

Implements and executes Veloxis's global Regulatory strategy. Understanding of strategic and tactical role and deliverables of global Regulatory strategy in the drug and device development and commercialization process. Experience with communicating the Regulatory strategy, issues, and risks in writ...

Eisai Inc.
Raleigh, North Carolina

The base salary range for the Associate Director, Global RWE (Real World Evidence), Global Medical Affairs - Neurology is from :181,000-237,600Under current guidelines, this position is eligible to participate in : Eisai Inc. This role primarily focuses on late-stage pipeline and marketed products, ...

Merz Aesthetics
Raleigh, North Carolina

The lead closely interacts with the Global Marketing, Global and Region Medical, and R&D teams to support registrational trials and provide leadership for global medical affairs sponsored and supported trials. The Associate Medical Director, Belotero Lead, provides oversight to the Strategic Directi...

Eisai Inc.
Durham, North Carolina

The base salary range for the Director, Real World Evidence, Global Medical Affairs is from :213,500-280,200Under current guidelines, this position is eligible to participate in : Eisai Inc. US medical affairs, HEOR, marketing, market access, global value and access teams, commercial) to prioritize ...

Chiesi Group
Cary, North Carolina

Accountable for global/regional regulatory strategies for new and existing products in collaboration with the Global Regulatory Team (GRT). The Global RA Manager contributes to the Company’s success by managing the Corporate R&D Pipeline (projects in R&D Development) by providing regulatory ...

Eisai
Durham, North Carolina

The base salary range for the Director, Real World Evidence, Global Medical Affairs is from :213,500-280,200Under current guidelines, this position is eligible to participate in : Eisai Inc. This role primarily focuses on late-stage pipeline and marketed products, interfaces with cross-functional te...