Global Regulatory Affairs Consultant | Clinical Submissions
Parexel
Parexel is seeking a Regulatory Affairs Consultant to guide global clinical development programs through the regulatory landscape. You will lead health authority engagements, submissions, and lifecycle management across US, EU, and other regions, partnering with cross-functional teams. The role emphasizes regulatory strategy, interactive stakeholder coordination, and a focus on successful approvals while maintaining compliance with FDA, EMA, ICH, and other global requirements. #J-18808-Ljbffr Parexel
Vacancy posted 1 day ago
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