Description

You will lead regulatory strategy for oncology programs at a late-stage clinical company developing RAS-targeted therapies. You'll ensure consistent, actionable regulatory advice across drug development teams and collaborate cross-functionally to align with company goals.

Requirements

• Degree in life sciences, pharmacy, medicine or related fields
• Minimum 12 years in pharma/biotech industry or relevant work experience
• Minimum 8 years in Regulatory Affairs including regulatory strategy and leadership roles
• Demonstrated success in leading regulatory submissions globally
• Direct experience with oncology drug development

Responsibilities

• Deliver sound regulatory strategy to program teams
• Motivate, mentor and develop direct reports
• Ensure drug development programs are fully resourced
• Anticipate upcoming work and ensure robust regulatory strategy support
• Establish collaborative relationships with cross-functional colleagues