Associate Program Director, Regulatory Affairs

IQVIA seeks an Associate Program Director for Regulatory Affairs to lead complex global regulatory programs for pharmaceutical and biotechnology clients. This strategic role oversees multiple workstreams, manages senior client relationships, and drives program governance and financial performance across the product development lifecycle.

Responsibilities

• Lead complex global Regulatory Affairs programs across multiple projects and functional teams
• Serve as strategic senior contact for clients and manage executive-level stakeholder relationships
• Establish program governance, oversight plans, KPIs and establish delivery frameworks
• Oversee cross-functional regulatory teams spanning strategy, operations, submissions and lifecycle management
• Monitor program performance, profitability and revenue realization with corrective action as needed

Requirements

• Bachelor's degree in Life Sciences, Pharmacy, Regulatory Affairs or related field
• Significant experience in Regulatory Affairs, Operations, or Strategy within CRO, pharma or biotech
• Proven track record leading large, complex global programs or portfolios
• Strong understanding of global regulatory frameworks and drug development processes
• Professional fluency in English and French, including client meeting leadership
• Experience managing client budgets, revenue forecasts and resource planning
• PMP, PRINCE2 or equivalent project management certification advantageous