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
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