Senior Manager, QPPV Office

• Own the pharmacovigilance agreement (PVA) management process
• Oversee and coordinate the timely preparation of authority-relevant documents
• Conceptualize and develop templates, project-specific documents, and processes

• At least two years of experience in global pharmacovigilance (not case processing), including specifically PVA management
• 4+ years of experience in pharmacovigilance, drug safety, epidemiology, risk management, scientific consulting, regulatory affairs, or a related field
• Bachelor's degree in life sciences, pharmacy, medicine, nursing, public health, epidemiology, regulatory affairs, or a related field, or equivalent experience required
• Certification in pharmacovigilance or drug safety preferred
• Certification in regulatory affairs, clinical safety preferred
• Certification in quality management or auditing preferred

• Benefit offerings outside the US may vary by country and will be aligned to local market practice
• Reasonable accommodations during the employment process for individuals with disabilities