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
Strategy Director, US Regulatory Affairs
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...
Associate Director, Global RWE (Real World Evidence), Global Medical Affairs - Neurology
The base salary range for the Associate Director, Global RWE (Real World Evidence), Global Medical Affairs - Neurology is from :181,000-237,600. US medical affairs, marketing, market access global value and access teams, commercial. US medical affairs, marketing, market access global value and acces...
Associate Director, US Regulatory Affairs Strategy
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...
Associate Director, Global RWE (Real World Evidence), Global Medical Affairs - Neurology
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, ...
Global Corporate Affairs Associate Director, Alzheimer’s disease
The candidate will report to the Executive Director for Global Corporate Affairs Alzheimer’s disease, with additional accountability to the International Therapy Area Leader. The Associate Director of Corporate Affairs (CA) for Alzheimer's disease will play a crucial role in supporting both the deve...
Director Quality Management
Oversight responsibility for all regulatory body surveys, such as, JCAHO, State Licensing Review, HCFA (CMS) Validation surveys. ...
Senior Director– Global Medical Affairs, Lilly Diabetes and Obesity
In addition, with input from the Director-Medical and Business Unit Team Physician/Regional Medical Leader, the CRP is responsible for assuring that his/her activities are clearly aligned with the strategic priorities of the respective business unit global Medical Affairs team, brand team(s), global...
Director, Global Sustainability & ESG Strategy
The Director, Global Sustainability & ESG Strategy is responsible for collaborating with key stakeholders to establish and maintain enterprise ESG requirements across Allegion’s global footprint. Director, Global Sustainability & ESG Strategy. This role will report to the Global Vice President, EHS,...
Sr. Director - Regulatory Affairs
We are a global healthcare leader headquartered in Indianapolis, Indiana. ...
Principal Regulatory Advisor, Global Regulatory Affairs, Innovation, Pharmaceuticals
Design and develop creative global regulatory strategy and technical regulatory documents based on interpretation of both regulatory and scientific information. Regulatory affairs experience, and understanding of the animal health industry and the animal drug development process. Strategic thinking ...