Associate Director, Global Case Intake & Submissions

A leading biotherapeutics company is looking for an Associate Director, Case Management Intake & Submissions to oversee safety data intake and submissions to regulators. The role requires at least 10 years of experience in clinical trial and pharmacovigilance, with strong leadership skills. The position involves monitoring compliance with global regulations and leading a team in a hybrid work schedule. Excellent analytical skills are crucial for success in this role. #J-18808-Ljbffr