Location: Remote

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 seasoned 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.

Key Responsibilities:

• Spearhead regulatory submissions for the oncology portfolio, driving strategy with precision and expertise.
• While focusing on a later-phase program, there may also be opportunities to contribute to early-phase studies depending on pipeline needs.
• Enjoy direct reporting lines to VP level, ensuring strategic insights are heard and valued.

Candidate Requirements:

• Minimum of 10 years in the industry, with at least 8 years dedicated to regulatory affairs.
• Proven track record in leading regulatory strategies through successful oncology submissions.
• Preferably from mid-to-large sponsors, not small biotech or CROs.
• Demonstrated ability to drive high-level regulatory strategy and navigate complex regulatory landscapes.

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 take your regulatory strategy career to the next level. Qualified candidates are encouraged to apply and help transform the future of oncology treatments.

Apply Now