Job Summary

A company is looking for a Senior Vice President, Regulatory Affairs.

Key Responsibilities:

• Develop and implement strategic plans for organization growth and provide regulatory advice for clinical development planning
• Lead teams in preparing regulatory strategies, reviewing clinical development plans, and building cross-functional alliances
• Manage Global Regulatory Affairs function, including staffing, resourcing, and supervision

Required Qualifications:

• Bachelor's degree in a scientific discipline, journalism, or English; MS or PhD preferred
• 16-18 years of related experience with a BA/BS, 14-16 years with an MA, or 12-14 years with a PhD in pharmaceutical, CRO, or biotechnology industry
• Minimum of 10-15 years managing people or processes in regulatory affairs
• Experience in preparing regulatory submissions in the US and Europe
• Experience working in multidisciplinary project teams