Senior Vice President, Regulatory Affairs

Overview

Role overseeing global regulatory strategy and submissions for drug development.

Ideal candidate should have 12+ years in Regulatory Affairs with experience in NDA submissions and FDA interactions.

Locations

• United States

Requirements

• Advanced degree preferred
• 12+ years in Regulatory Affairs
• Proven track record of NDA submissions

Responsibilities

• Lead global regulatory function
• Develop regulatory strategy
• Manage regulatory submissions
• Serve as primary regulatory contact
• Build relationships with regulatory agencies
• Provide expert regulatory input
• Support risk assessments
• Guide project teams

Benefits

• Medical benefits
• Dental benefits
• Vision benefits
• 401K
• Time off
• Incentive plans