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Job Description
- Receives, follows-up, and reports spontaneous reports of adverse events (AEs) and other safety information
- Receives, follow-ups, and reports product quality complaints (PQCs) and medical information enquiries (MIEs) and checks for hidden AEs
- Communicates and performs reconciliation with relevant PV staff, partners and third party service providers
- Prepares periodic safety update reports (PSURs) and risk management plans (RMPs)
- Prepares/reviews the safety data exchange agreements (SDEAs)
- Performs literature searching for assigned products and therapeutic areas
- Conducts PV training for country-based staff
- Performs archiving of PV documentation
Job Requirements
- Bachelor Degree of Medicine or Pharmacy
- Specialty in any medical field is a plus
