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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Senior Manager Regulatory Strategy Oncology & Japan Affairs - Regulatory Affairs

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeTokyo, JapanNo salary listed

About the Job

Requirements

  • Bachelor's degree in a scientific discipline.
  • At least 10 years of pharmaceutical industry experience and at least 5 years of relevant regulatory experience.
  • Experience managing health authority interactions, major submissions, and approvals in Japan.
  • Deep knowledge of Japan submission requirements, local regulations, and regulatory standards.
  • Knowledge of clinical trial requirements and the ability to resolve local procedural challenges.
  • Experience supporting business start-up activities.
  • Ability to ensure compliance with Japan regulatory requirements and local standards.
  • Strategic thinking and commercial awareness.
  • Strong written and verbal communication skills.
  • Ability to thrive in and foster effective matrix teamwork in a global environment.
  • Fluency in Japanese and English.

Responsibilities

  • Plan and execute Japan regulatory strategies and PMDA consultations for assigned programs.
  • Lead marketing application and post-approval change submissions.
  • Partner with local and global leadership to support Regulatory Affairs operations.
  • Manage interactions with PMDA and other Japanese health authorities.
  • Lead or support clinical trial notification preparation and submission activities.
  • Represent Regulatory Affairs within clinical, commercial, medical, and patient safety teams.
  • Support local labeling, patient information, and promotional material review activities.

Desired Qualifications

  • Master's degree.

About the Company

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company size
10,001+
Company stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988

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