Associate Program Director, Regulatory Affairs w… - Jobeax
Opis oferty
Associate Program Director, Regulatory Affairs w Warszawa, Polska
IQVIA
Warszawa, Polska
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
Twój zakres obowiązków - Zarządzanie przypisanymi procesami i projektami regulacyjnymi, w tym ich wdrażaniem, monitorowaniem, komunikacją i zapewnieniem zgodności. - Współpraca z właścicielami procesów i ekspertami regulacyjnymi przy opracowywaniu, monitorowaniu, raportowaniu i ocenie globalnych wskaźników KPI.
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