Safety Expert

Há 2 dias

São Paulo, São Paulo, Brasil beBeePharmacovigilance Tempo inteiro R$48.000 - R$86.000
Pharmacovigilance Professional Role

We are seeking highly skilled and detail-oriented Pharmacovigilance professionals to join our dynamic team. In this role, you will be responsible for reviewing and processing safety events, performing literature searches, and generating data listings.

Key Responsibilities:
  • Review and process safety events including pre-marketing, post-marketing, medical device, and drug-related information according to project procedures
  • Perform literature searches to identify safety information from abstracts and full articles for both pre and post-marketed products
  • Generate accurate data listings from the safety database and maintain the integrity of the data
  • Complete adverse event follow-up in writing and/or by phone as required
  • Contribute to the development and review of relevant safety tracking systems and assist with maintaining project files
  • Participate in safety reviews of clinical and diagnostic data as part of case processing
  • Collaborate on the development of Safety Management Plans, including the creation of specific processes to ensure consistency within the project
Requirements:
  • 1-4 years of experience in Pharmaceutical/CRO environment depending on position
  • Excellent verbal and written communication skills
  • Detail-oriented and organized
  • Fluent in written and verbal English
  • Ability to work independently and effectively within a team environment

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