Global Regulatory Lead For Pharma Submissions
Há 4 dias
Vila Fria, Portuguese Republic, Portugal
IQVIA LLC
Tempo integral
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IQVIA is seeking an experienced Associate Director, Regulatory Affairs to lead complex global regulatory projects for pharmaceutical and biotechnology clients. This is a client-facing individual contributor role focused on regulatory strategy, regulatory submissions, project leadership, and health authority interactions across global development programs.
You will guide regulatory strategy, oversee submission documents such as INDs, IMPDs, BLA/NDAs/MAAs, and collaborate with cross-functional
You will guide regulatory strategy, oversee submission documents such as INDs, IMPDs, BLA/NDAs/MAAs, and collaborate with cross-functional