Primary Responsibilities:

  • Carry out case processing activities;
  • Review, rank, verify, process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency.  Process cases based on these assessments;
  • Liaise with key partners, locally , and other stakeholders regarding safety data collection and data reconciliation;
  • Develop and maintain expertise and knowledge for applicable corporate and global regulations, for guidelines, Standard Operating Procedures, for data entry conventions, and for search functions in the safety database;
  • Determine reportability of scheduled reports , ensuring adherence to regulatory requirements;
  • Consistently apply regulatory requirements and Pfizer policies;
  • Participate, as appropriate, in local, internal and external safety activities;
  • Knowledge and application of local regulation;
  • Assessment and submission of adverse event reports to Health Authorities.


Technical Skill Requirements

  • Experience in pharmacovigilance and/or data management;
  • Experience and skill with medical writing an advantage;
  • Health Care Professional or equivalent experience;
  • Fluency in spoken and written English.


Data máxima para inscrição á vaga: 17/02