Join Takeda as a Director, Global Regulatory Lead Oncology where you will be part of the global regulatory team. As Director, Global Regulatory Lead Oncology you will set global regulatory strategy and lead major submissions for high-impact oncology programs.
Requirements
- Bachelor’s Degree required, scientific discipline strongly preferred, advanced degree in a scientific discipline strongly preferred.
- A minimum of 8 years of pharmaceutical industry experience, inclusive of regulatory and/or related experience.
- Solid working knowledge of drug development process and regulatory requirements. Knowledge of FDA is a must. Knowledge of EU, Canada, ROW is a plus.
- Experience in managing major regulatory filing(s); and experience as a significant contributor to regulatory and/or development strategies
- Understand and interpret complex scientific issues across multiple projects as it relates to regulatory requirements and strategy.
- Strong oral and written communications, managing and adhering to timelines, negotiation skills, integrity and adaptability.
Benefits
- Short-term and/or long-term incentives
- Medical, dental, vision insurance
- 401(k) plan and company match
- Short-term and long-term disability coverage
- Basic life insurance
- Tuition reimbursement program
- Paid volunteer time off
- Company holidays
- Well-being benefits
- Up to 80 hours of sick time
- Up to 120 hours of paid vacation
