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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