Associate Director, Case Management & Submissions (Hybrid)

A leading global biotherapeutics firm is seeking an Associate Director for Case Management Intake & Submissions. This hybrid role emphasizes oversight of incoming safety data, monitoring regulatory submissions, and ensuring compliance with reporting requirements. Candidates must possess a strong background in Clinical Trial and Post-marketing Pharmacovigilance, alongside leadership experience. The role involves significant analysis of complex regulatory intelligence and collaboration across teams to support process improvements. Exceptional candidates will demonstrate their capacity to lead high-impact projects effectively. #J-18808-Ljbffr