Senior Director, Global Regulatory Lead

GSK

Belgium
Base: $221,925 to $369,875 (us); bonus/equity: ann...
Hybrid
7+ years drug development regulatory experience
Leading submission and approval activities
Managing global regulatory interactions with health authorities
GSK is seeking a Senior Director, Global Regulatory Lead to develop and execute regulatory strategies for drug development, ensuring compliance with internal and external standards. The role requires extensive experience in regulatory affairs and leadership capabilities, focusing on delivering impactful medicines to patients

Job Summary

  • The role is accountable for developing and executing regulatory strategies to ensure development programs meet the needs of key markets and the Medicine Profile.
  • Candidates must have extensive experience leading development, submission, and approval activities with a proven track record of successful relationships with Health Authorities.
  • This position offers a competitive annual base salary ranging from $221,925 to $369,875 for US hires, along with an annual bonus and share-based long-term incentive program.

Matching Summary

Match Score: 85

GSK is seeking a Senior Director, Global Regulatory Lead to develop and execute regulatory strategies for drug development, ensuring compliance with internal and external standards. The role requires extensive experience in regulatory affairs and leadership capabilities, focusing on delivering impactful medicines to patients.

Salary

Base: $221,925 to $369,875 (US); Bonus/Equity: Annual bonus and share-based long term incentive; Benefits: Health care, retirement, paid holidays, vacation, and parental leave

Skills & Requirements

Must-have

  • 7+ years drug development regulatory experience
  • Leading submission and approval activities
  • Managing global regulatory interactions with Health Authorities
  • Developing regulatory strategy for key markets
  • Matrix working with VP level stakeholders

Nice-to-have

  • Experience building or scaling regulatory teams
  • Fluency in European languages like French or Dutch
  • Track record of lifecycle management and variations
  • Advanced degree in life sciences or related field
  • Experience in business development due diligence

Key Requirements

  • Bachelor's degree in life sciences, pharmacy, medicine or related discipline
  • 7+ years of experience in all phases of drug development process
  • Extensive knowledge of clinical trial and licensing requirements in priority markets
  • Proven experience leading regulatory activities outside local region

Work Rights

Not specified

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