Description
Job Summary:
This professional will support the analysis of regulations, development of procedures, extraction of data, and recording of adverse events in pharmacovigilance.
Key Highlights:
1. Will support the analysis of pharmacovigilance resolutions and ordinances
2. Will assist in the development, review, and implementation of internal procedures
3. Will participate in audits and regulatory inspections
Description:
* Currently pursuing a bachelor's degree in Pharmaceutical Sciences, Biomedicine, or Nursing;
* Intermediate English proficiency;
* Intermediate proficiency in Microsoft Office suite;
* Prior experience in pharmacovigilance or technical documentation within the pharmaceutical industry is desirable;
* Willingness to travel occasionally;
* Availability to work Monday through Friday, from 8:00 AM to 5:00 PM, in Itapira/SP.
* Support the analysis of pharmacovigilance-related resolutions and ordinances;
* Assist in the development, review, and implementation of internal procedures;
* Extract data from the pharmacovigilance database and collaborate on drafting legal documents and internal reports;
* Perform collection and registration of adverse events in the database, assessing causality when necessary;
* Participate in activities related to internal/external audits and regulatory inspections.
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