Global Regulatory Strategy Director, Neuroscience

Regulatory Jobs

Princeton (NJ)

On-site

USD 227,000 - 275,000

Full time

14 days+

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Benefits offered by this job

Wellbeing support
Flexible Time Off
Company holidays
Paid vacation
Global Shutdown

Job summary

Bristol Myers Squibb seeks a Sr Director, Global Regulatory Strategy in Neuroscience to lead regulatory strategy development, coordinate across projects, and liaise with health authorities worldwide. The role drives global regulatory plans, supports due diligence, and partners with US and international teams to influence development and commercialization decisions.

Ideal candidates bring advanced scientific degrees with 8–12 years in pharma regulatory affairs, including global experience in

Qualifications

  • Advanced degree in scientific discipline; MD, PhD or PharmD preferred.
  • 8–12 years pharma industry experience, including 6–8 years in regulatory affairs.
  • Global regulatory experience with US/EU background is highly preferred.
  • Expertise in Drug Development/CMC/Pharmtox/Biopharmaceutics/Clinical/Promotional areas.

Responsibilities

  • Develop global regulatory strategies and plans for identified projects/assets.
  • Interface with health authorities and serve as primary global point person for assigned projects.
  • Lead regulatory submissions and align strategies across Neuroscience programs.
  • Collaborate with regional staff on global/regional regulatory activities.

Skills

Regulatory leadership
Global regulatory
Neurology experience
US/EU regulatory
Strategic thinking
Leadership
Communication

Education

Advanced degree in science (MD/PhD/PharmD)

Job description

Bristol Myers Squibb seeks a Sr Director, Global Regulatory Strategy in Neuroscience to lead regulatory strategy development, coordinate across projects, and liaise with health authorities worldwide. The role drives global regulatory plans, supports due diligence, and partners with US and international teams to influence development and commercialization decisions.

Ideal candidates bring advanced scientific degrees with 8–12 years in pharma regulatory affairs, including global experience in

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