IQVIA in Barcelona is seeking a Director of Regulatory Affairs to lead regulatory strategy and project management for drug development. The ideal candidate will have a Master’s degree in Life Sciences and at least 8 years of regulatory experience in both US and EU markets. Responsibilities include authoring key regulatory submissions, providing project leadership, and mentoring junior team members. This role requires strong client-facing skills and experience leading complex, cross-functional teams to drive drug development projects successfully.
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