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

Para se candidatar a esta vaga cadastre seu currículo em https://ferring.wd3.myworkdayjobs.com/en-US/Ferring/job/Ferring-Brazil/Pharmacovigilance-Analyst_R0011233-1