Pharmacovigilance Country Head PE/VE Collects adverse event data on all marketed products and those in development.
Implements and oversees adverse event processes and databases.
Ensures regulatory compliance for both expedited and periodic reports.
Provides integrated strategic safety expertise to clinical development programs.
Performs active pharmacovigilance with rapid identification and analysis of safety signals to define emerging drug safety profiles of all products and drive patient risk management.
Delivers high-quality product safety data and analysis to internal and external customers throughout the product life cycle.
Education Advanced life sciences degree, preferably medical doctor,



or equivalent through experience Experience Minimum of 3-5 years of experience in a (general) healthcare organization, especially in Clinical Development and/or Medical Affairs and/or Pharmacovigilance Preferably in-depth experience in drug development process across different stages, especially clinical development and clinical operations Experience in development and authorship of complex PV documents Experience of leading and contributing to teams across cultures and geographies (if applicable) Experience of working across and building effective working relationships between functions Skills

📌 Pharmacovigilance Country Head Pe/Ve (Callao)
🏢 Bayer
📍 Callao