Graduate Pharmacovigilance Associate

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As a Graduate Pharmacovigilance Associate you will be joining the world’s largest and most comprehensive clinical research organisation, powered by healthcare intelligence.

Responsibilities

• Receives and processes individual case safety reports (ICSRs) including serious adverse events, adverse events of special interest, and suspected adverse drug reactions from clinical trials, spontaneous reports and published reports. This includes tracking of received ICSR, entry of ICSR into company or client safety database and query management.
• Performs consistent coding of diseases, adverse events, and medications according to project-specific coding conventions in the Safety Database.
• Assesses reportability of ICSRs based on the project-specific Safety Reporting Assessment sheet.
• Submits safety reports to Regulatory Authorities, I...