Global Regulatory Strategy Director, Neuroscience

Bristol-Myers Squibb Co; Princeton (NJ); On-site; USD 227,000 - 275,000; Full time

Benefits offered by this job

Health coverage

Wellbeing programs

Flexible work options

Job summary

Bristol Myers Squibb is seeking a Senior Director, Global Regulatory Lead for Neuroscience in Princeton, NJ. The role will shape global regulatory strategies across development assets and marketed products, coordinating with regional teams and health authorities.

You will serve as the primary global regulatory point person, provide strategic counsel to development and commercialization teams, and drive submissions and regulatory planning in a fast-paced environment focused on neurology and

Qualifications

• Advanced degree in scientific discipline; MD/PhD/PharmD preferred, neurology focus preferred.
• 8-12 years pharmaceutical industry experience, including 6-8 years in regulatory affairs; global experience preferred.
• Strong knowledge of drug development, regulatory processes, US/EU experience.

Responsibilities

• Lead global regulatory strategies and plans for investigational and marketed products.
• Serve as regulatory representative on company-wide projects and initiatives.
• Collaborate with regional regulatory staff as Global Lead and US Regional Lead.
• Interface with health authorities on assigned projects.
• Oversee submissions with regulatory product managers and operations teams.
• Monitor regulatory landscape and advise on impact to projects.

Skills

Regulatory leadership

Global regulatory strategy

US regulatory experience

Cross-functional collaboration

Strategic counseling

Education

MD/PhD/PharmD

Job description

Bristol Myers Squibb is seeking a Senior Director, Global Regulatory Lead for Neuroscience in Princeton, NJ. The role will shape global regulatory strategies across development assets and marketed products, coordinating with regional teams and health authorities.

You will serve as the primary global regulatory point person, provide strategic counsel to development and commercialization teams, and drive submissions and regulatory planning in a fast-paced environment focused on neurology and