A pioneering pharmaceutical company is looking for a Regulatory Affairs Senior Manager. The selected candidate will work with global teams to define regulatory strategies and manage the submission of regulatory documents.
Responsibilities:
- Define development and regulatory strategy with local and global teams
- Lead or support regulatory and CRO activities for specific products
- Provide strategic regulatory advice as a member of global regulatory teams
- Coordinate and respond to regulatory authorities' inquiries within strict deadlines
- Maintain and organise regulatory files per internal standards
- Review and recommend changes to regulatory documentation and processes
Requirements:
- Bachelor’s degree or above (advanced science or healthcare degree is a plus)
- More than 5 years of experience in regulatory affairs and clinical development role
- Experience in interpretation of guidelines
- Prior experience with regulatory filings (electronic submissions)
- Knowledge of regulations
- Excellent technical system skills
- Native level Japanese; business level English
About the Company:
A pioneering pharmaceutical company focused on advancing innovative therapeutic solutions. Committed to scientific excellence, it aims to improve patient outcomes through cutting-edge research and development.
Keywords:
製薬, メディカル, サイエンス, 求人, 外資系
2094470/001