Director, Global Regulatory Affairs

Become part of our team as Director, Global Regulatory Affairs, leading the development and strategy for neurology and oncology product registrations. Oversee regulatory submissions, collaborate with cross-functional teams, and ensure compliance. Ideal for experienced professionals with a strong background in regulatory affairs within the life sciences sector.

Skills

• regulatory strategy
• regulatory submission
• fda submissions
• project management
• cross-functional leadership
• regulatory compliance
• scientific data interpretation
• regulatory intelligence
• orphan drug designation
• protocol amendments
• regulatory strategy development
• stakeholder management
• regulatory negotiation
• life sciences industry knowledge
• mentoring
• resource allocation
• vendor management
• budget management
• regulatory reporting
• regulatory liaison
• strategic planning
• regulatory strategy team leadership
• regulatory strategy team management