Job Description:

  • Perform daily screening of all adverse event reports and safety information notification.
  • Process the adverse event / safety information notification and submit the cases to headquarters and health authorities.
  • Ensure follow-up of severe cases as well as of drug exposure of pregnant patients.
  • Assist in planning and elaborating the Periodic Pharmacovigilance Reports with the headquarters, as well as ensure their proper submission to the health authority.
  • Assist in Pharmacovigilance training conducted for all employees of the company and for new employees.
  • Attend meetings with pharmaceuticals associations.
  • Ensure the maintenance of Pharmacovigilance files.
  • Prepare statistical reports of the area.
  • Perform periodic monitoring of local literature to search adverse event cases and safety information.
  • Search scientific articles in the literature according to the requests of healthcare professionals, as well as address the doubts properly according to the established in SOP.
  • Search scientific articles in the literature supporting Marketing and Medical Departments.
  • Assist in processing technical complaints in support of the Call Center and the Quality Department.
  • Assist in drafting and updating Standard Operating Procedures.


Location: Ferring Brazil



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