Ingrid catalina Rincon pardo

Pharmacovigilance AnalystFull Time

• Job Details:Report Serious, not serious, Spontaneous and case tracking patients in clinical studies adverse events.  Review of the Documents applicable to Pharmacovigilance Department: Local legislation, procedures and review of literature.  Review and control of the documents submitted daily to INVIMA (FOREAM and SUSARs).  Support internal and external processes of pharmacovigilance audits.  Support training processes and training company personnel in pharmacovigilance.  Search medical databases of articles for the identification and registration of adverse events.  Submission of Adverse Events in Clinical Trials.  Document management.  Audit calls for monitoring of patients involved in the different clinical trials.  Sending documentation related to the regulatory authority Adverse Events.  Review, ship and handling of SUSARs.  Review of Local SOPs Pharmacovigilance and clinical trials.