Jr Assoc Pharmocovigilance

About the role

As Jr Assoc Pharmacovigilance, you will help make sure safety information reaches the right people at the right time. You will process adverse events and product quality complaints, support timely reporting to local Health Authorities and keep safety records accurate and inspection-ready. Working in International Operations, you will turn every report into reliable data that supports people using Novo treatments and strengthens pharmacovigilance operations.

What you'll do

• Be part of the local safety process from first report to closure, working under appropriate supervision while building your own expertise
• Receive, document and report adverse events (AEs), product quality complaints (PQCs) and AEs associated with PQCs to Global Safety within required timelines
• Monitor the safety mailbox and handle safety information and customer complaints received by phone, through digital applications and via internal safety portals
• Carry out assigned activities across the ICSR lifecycle in Veeva Safety and Veeva Quality, from intake, assessment and case narrative preparation to quality review
• Perform quality checks, source data verification and reconciliations, so cases are accurate, complete and consistent

What you need

• 1–2 yrs of experience
• Pharmacovigilance
• Clinical research
• Documentation
• Communication
• Reconciliation
• M.Pharm