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

CANDIDATE-SE