Impress employers and recruiters.
Choose from hundreds of resume examples.

Impress employers and recruiters.
Choose from hundreds of resume examples.

Target Resume Now

About the Role

Lead Japan regulatory strategies across multiple therapeutic areas while collaborating with global regulatory teams and local cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

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
• Build strong partnerships across a global matrix environment

Requirements

• Bachelor's degree in a scientific discipline; Master's degree preferred
• 10+ years in the pharmaceutical industry and 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 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, commercial awareness, and strong written and verbal communication skills
• Ability to thrive in and foster effective matrix teamwork in a global environment
• Fluent Japanese and English language skills

Skills

• Strategic thinking
• Commercial awareness
• Strong written communication
• Strong verbal communication
• Matrix teamwork

Location

• Japan

Work Type

• Hybrid

Experience Level

• Senior Manager
• 10+ years in the pharmaceutical industry
• 5+ years of relevant regulatory experience

Education Level

• Bachelor's degree in a scientific discipline
• Master's degree preferred

Benefits

• Annual bonuses or other incentive plans
• Equity awards
• Pension or retirement benefits
• 401(k) company match
• Health and wellness programs
• Fitness centers
• Insurance benefits (e.g. medical, dental, vision, life and disability)
• Paid time off
• Family support benefits

About the Company

• Regeneron uses science and innovation to develop life-changing medicines for people with serious diseases.
• We are committed to building a workplace with an inclusive culture.

Equal Opportunity

• Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.
• Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.